Canonical Allele Identifier: CA413424598

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717543G>A , CM000685.2:g.67717543G>A	GRCh38
NC_000023.10:g.66937385G>A , CM000685.1:g.66937385G>A	GRCh37
NC_000023.9:g.66854110G>A	NCBI36
NG_009014.2:g.178512G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000044.6:c.2239G>A MANE Select	NP_000035.2:p.Val747Met
ENST00000374690.9:c.2239G>A MANE Select	ENSP00000363822.3:p.Val747Met
NM_000044.3:c.2239G>A	NP_000035.2:p.Val747Met
NM_000044.4:c.2239G>A	NP_000035.2:p.Val747Met
NM_001011645.2:c.643G>A	NP_001011645.1:p.Val215Met
NM_001011645.3:c.643G>A	NP_001011645.1:p.Val215Met
ENST00000374690.7:c.2239G>A	ENSP00000363822.3:p.Val747Met
ENST00000396043.2:c.643G>A	ENSP00000379358.2:p.Val215Met
ENST00000396043.3:c.866G>A	ENSP00000379358.3:n.866G>A
ENST00000396043.4:c.*587G>A	ENSP00000379358.4:n.*587G>A
ENST00000396044.7:c.2173+5854G>A	ENSP00000379359.3:n.2173+5854G>A
ENST00000396044.8:c.2173+5854G>A	ENSP00000379359.3:n.2173+5854G>A
ENST00000612452.4:c.1669G>A	ENSP00000484033.1:p.Val557Met
ENST00000612452.5:c.2239G>A	ENSP00000484033.2:p.Val747Met