Canonical Allele Identifier: CA413426718

Gene: AR

Linked Data

• COSMIC: COSM150792
• MyVariant Identifiers: chrX:g.66941738G>T (hg19) ; chrX:g.67721896G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721896G>T , CM000685.2:g.67721896G>T	GRCh38
NC_000023.10:g.66941738G>T , CM000685.1:g.66941738G>T	GRCh37
NC_000023.9:g.66858463G>T	NCBI36
NG_009014.2:g.182865G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*730G>T	ENSP00000379358.4:n.*730G>T
ENST00000374690.9:c.2382G>T MANE Select	ENSP00000363822.3:p.Glu794Asp
ENST00000396043.3:c.1009G>T	ENSP00000379358.3:n.1009G>T
ENST00000396044.8:c.2174-1790G>T	ENSP00000379359.3:n.2174-1790G>T
ENST00000612452.5:c.2382G>T	ENSP00000484033.2:p.Glu794Asp
ENST00000374690.7:c.2382G>T	ENSP00000363822.3:p.Glu794Asp
ENST00000396043.2:c.786G>T	ENSP00000379358.2:p.Glu262Asp
ENST00000396044.7:c.2174-1790G>T	ENSP00000379359.3:n.2174-1790G>T
ENST00000612452.4:c.1812G>T	ENSP00000484033.1:p.Glu604Asp
NM_000044.3:c.2382G>T	NP_000035.2:p.Glu794Asp
NM_001011645.2:c.786G>T	NP_001011645.1:p.Glu262Asp
NM_000044.4:c.2382G>T	NP_000035.2:p.Glu794Asp
NM_001011645.3:c.786G>T	NP_001011645.1:p.Glu262Asp
NM_000044.6:c.2382G>T MANE Select	NP_000035.2:p.Glu794Asp