Canonical Allele Identifier: CA413428200
Community Standard Title: NM_000044.6(AR):c.2631C>G (p.Phe877Leu)
Gene: AR HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67723709C>G , CM000685.2:g.67723709C>G GRCh38
NC_000023.10:g.66943551C>G , CM000685.1:g.66943551C>G GRCh37
NC_000023.9:g.66860276C>G NCBI36
NG_009014.2:g.184678C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000044.6:c.2631C>G MANE Select NP_000035.2:p.Phe877Leu
ENST00000374690.9:c.2631C>G MANE Select ENSP00000363822.3:p.Phe877Leu
NM_000044.3:c.2631C>G NP_000035.2:p.Phe877Leu
NM_000044.4:c.2631C>G NP_000035.2:p.Phe877Leu
NM_001011645.2:c.1035C>G NP_001011645.1:p.Phe345Leu
NM_001011645.3:c.1035C>G NP_001011645.1:p.Phe345Leu
ENST00000374690.7:c.2631C>G ENSP00000363822.3:p.Phe877Leu
ENST00000396043.2:c.1035C>G ENSP00000379358.2:p.Phe345Leu
ENST00000396043.3:c.1258C>G ENSP00000379358.3:n.1258C>G
ENST00000396043.4:c.*979C>G ENSP00000379358.4:n.*979C>G
ENST00000396044.7:c.2197C>G ENSP00000379359.3:p.His733Asp
ENST00000396044.8:c.2197C>G ENSP00000379359.3:p.His733Asp
ENST00000612452.4:c.2082C>G ENSP00000484033.1:p.Phe694Leu
ENST00000612452.5:c.2631C>G ENSP00000484033.2:p.Phe877Leu
Search 100 bp 5'
Search 100 bp 3'