Canonical Allele Identifier: CA399302271
Community Standard Title: NM_004448.4(ERBB2):c.2191T>G (p.Phe731Val)
Gene: ERBB2 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NM_004448.4:c.2191T>G MANE Select NP_004439.2:p.Phe731Val
ENST00000269571.10:c.2191T>G MANE Select ENSP00000269571.4:p.Phe731Val
NM_001005862.2:c.2101T>G , LRG_724t1:c.2101T>G NP_001005862.1:p.Phe701Val
NM_001005862.3:c.2101T>G NP_001005862.1:p.Phe701Val
NM_001289936.1:c.2146T>G , LRG_724t4:c.2146T>G NP_001276865.1:p.Phe716Val
NM_001289936.2:c.2146T>G NP_001276865.1:p.Phe716Val
NM_001289937.1:c.2191T>G NP_001276866.1:p.Phe731Val
NM_001289937.2:c.2191T>G NP_001276866.1:p.Phe731Val
NM_001382782.1:c.2101T>G NP_001369711.1:p.Phe701Val
NM_001382783.1:c.2101T>G NP_001369712.1:p.Phe701Val
NM_001382784.1:c.2308T>G NP_001369713.1:p.Phe770Val
NM_001382785.1:c.2293T>G NP_001369714.1:p.Phe765Val
NM_001382786.1:c.2289+19T>G NP_001369715.1:n.2289+19T>G
NM_001382787.1:c.2266T>G NP_001369716.1:p.Phe756Val
NM_001382788.1:c.2221T>G NP_001369717.1:p.Phe741Val
NM_001382789.1:c.2212T>G NP_001369718.1:p.Phe738Val
NM_001382790.1:c.2188T>G NP_001369719.1:p.Phe730Val
NM_001382791.1:c.2182T>G NP_001369720.1:p.Phe728Val
NM_001382792.1:c.2172+19T>G NP_001369721.1:n.2172+19T>G
NM_001382793.1:c.2166+25T>G NP_001369722.1:n.2166+25T>G
NM_001382794.1:c.2149T>G NP_001369723.1:p.Phe717Val
NM_001382795.1:c.2143T>G NP_001369724.1:p.Phe715Val
NM_001382796.1:c.2191T>G NP_001369725.1:p.Phe731Val
NM_001382797.1:c.2191T>G NP_001369726.1:p.Phe731Val
NM_001382798.1:c.2191T>G NP_001369727.1:p.Phe731Val
NM_001382799.1:c.2011T>G NP_001369728.1:p.Phe671Val
NM_001382800.1:c.2191T>G NP_001369729.1:p.Phe731Val
NM_001382801.1:c.2143T>G NP_001369730.1:p.Phe715Val
NM_001382802.1:c.1933T>G NP_001369731.1:p.Phe645Val
NM_001382803.1:c.2166+25T>G NP_001369732.1:n.2166+25T>G
NM_001382804.1:c.1363T>G NP_001369733.1:p.Phe455Val
NM_001382805.1:c.2191T>G NP_001369734.1:p.Phe731Val
NM_001382806.1:c.1223-321T>G NP_001369735.1:n.1223-321T>G
NM_004448.3:c.2191T>G , LRG_724t2:c.2191T>G NP_004439.2:p.Phe731Val
NR_110535.1:n.2515T>G
NR_110535.2:n.2429T>G
ENST00000269571.9:c.2191T>G ENSP00000269571.4:p.Phe731Val
ENST00000406381.6:c.2101T>G ENSP00000385185.2:p.Phe701Val
ENST00000445658.6:c.1363T>G ENSP00000404047.2:p.Phe455Val
ENST00000541774.5:c.2146T>G ENSP00000446466.1:p.Phe716Val
ENST00000578373.5:c.*1981T>G ENSP00000463427.1:n.*1981T>G
ENST00000578630.1:n.800T>G
ENST00000580074.1:c.297T>G
ENST00000582818.5:c.490+19T>G
ENST00000583038.5:n.3325T>G
ENST00000584450.5:c.2191T>G ENSP00000463714.1:p.Phe731Val
ENST00000584601.5:c.2101T>G ENSP00000462438.1:p.Phe701Val
XM_024450641.1:c.2329T>G XP_024306409.1:p.Phe777Val
XM_024450642.1:c.2284T>G XP_024306410.1:p.Phe762Val
XM_024450643.1:c.2239T>G XP_024306411.1:p.Phe747Val