Canonical Allele Identifier: CA399302267
Community Standard Title: NM_004448.4(ERBB2):c.2191T>A (p.Phe731Ile)
Gene: ERBB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39723643T>A , CM000679.2:g.39723643T>A GRCh38
NC_000017.10:g.37879896T>A , CM000679.1:g.37879896T>A GRCh37
NC_000017.9:g.35133422T>A NCBI36
NG_007503.1:g.40504T>A , LRG_724:g.40504T>A

Transcript Alleles

HGVS Amino-acid Change
NM_004448.4:c.2191T>A MANE Select NP_004439.2:p.Phe731Ile
ENST00000269571.10:c.2191T>A MANE Select ENSP00000269571.4:p.Phe731Ile
NM_001005862.2:c.2101T>A , LRG_724t1:c.2101T>A NP_001005862.1:p.Phe701Ile
NM_001005862.3:c.2101T>A NP_001005862.1:p.Phe701Ile
NM_001289936.1:c.2146T>A , LRG_724t4:c.2146T>A NP_001276865.1:p.Phe716Ile
NM_001289936.2:c.2146T>A NP_001276865.1:p.Phe716Ile
NM_001289937.1:c.2191T>A NP_001276866.1:p.Phe731Ile
NM_001289937.2:c.2191T>A NP_001276866.1:p.Phe731Ile
NM_001382782.1:c.2101T>A NP_001369711.1:p.Phe701Ile
NM_001382783.1:c.2101T>A NP_001369712.1:p.Phe701Ile
NM_001382784.1:c.2308T>A NP_001369713.1:p.Phe770Ile
NM_001382785.1:c.2293T>A NP_001369714.1:p.Phe765Ile
NM_001382786.1:c.2289+19T>A NP_001369715.1:n.2289+19T>A
NM_001382787.1:c.2266T>A NP_001369716.1:p.Phe756Ile
NM_001382788.1:c.2221T>A NP_001369717.1:p.Phe741Ile
NM_001382789.1:c.2212T>A NP_001369718.1:p.Phe738Ile
NM_001382790.1:c.2188T>A NP_001369719.1:p.Phe730Ile
NM_001382791.1:c.2182T>A NP_001369720.1:p.Phe728Ile
NM_001382792.1:c.2172+19T>A NP_001369721.1:n.2172+19T>A
NM_001382793.1:c.2166+25T>A NP_001369722.1:n.2166+25T>A
NM_001382794.1:c.2149T>A NP_001369723.1:p.Phe717Ile
NM_001382795.1:c.2143T>A NP_001369724.1:p.Phe715Ile
NM_001382796.1:c.2191T>A NP_001369725.1:p.Phe731Ile
NM_001382797.1:c.2191T>A NP_001369726.1:p.Phe731Ile
NM_001382798.1:c.2191T>A NP_001369727.1:p.Phe731Ile
NM_001382799.1:c.2011T>A NP_001369728.1:p.Phe671Ile
NM_001382800.1:c.2191T>A NP_001369729.1:p.Phe731Ile
NM_001382801.1:c.2143T>A NP_001369730.1:p.Phe715Ile
NM_001382802.1:c.1933T>A NP_001369731.1:p.Phe645Ile
NM_001382803.1:c.2166+25T>A NP_001369732.1:n.2166+25T>A
NM_001382804.1:c.1363T>A NP_001369733.1:p.Phe455Ile
NM_001382805.1:c.2191T>A NP_001369734.1:p.Phe731Ile
NM_001382806.1:c.1223-321T>A NP_001369735.1:n.1223-321T>A
NM_004448.3:c.2191T>A , LRG_724t2:c.2191T>A NP_004439.2:p.Phe731Ile
NR_110535.1:n.2515T>A
NR_110535.2:n.2429T>A
ENST00000269571.9:c.2191T>A ENSP00000269571.4:p.Phe731Ile
ENST00000406381.6:c.2101T>A ENSP00000385185.2:p.Phe701Ile
ENST00000445658.6:c.1363T>A ENSP00000404047.2:p.Phe455Ile
ENST00000541774.5:c.2146T>A ENSP00000446466.1:p.Phe716Ile
ENST00000578373.5:c.*1981T>A ENSP00000463427.1:n.*1981T>A
ENST00000578630.1:n.800T>A
ENST00000580074.1:c.297T>A
ENST00000582818.5:c.490+19T>A
ENST00000583038.5:n.3325T>A
ENST00000584450.5:c.2191T>A ENSP00000463714.1:p.Phe731Ile
ENST00000584601.5:c.2101T>A ENSP00000462438.1:p.Phe701Ile
XM_024450641.1:c.2329T>A XP_024306409.1:p.Phe777Ile
XM_024450642.1:c.2284T>A XP_024306410.1:p.Phe762Ile
XM_024450643.1:c.2239T>A XP_024306411.1:p.Phe747Ile