Canonical Allele Identifier: CA10436604

Gene: AR

Linked Data

• dbSNP Id: rs773708434
• ExAC: X:66937352 G / A
• gnomAD v2: X-66937352-G-A
• gnomAD v4: X-67717510-G-A
• MyVariant Identifiers: chrX:g.66937352G>A (hg19) ; chrX:g.67717510G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717510G>A , CM000685.2:g.67717510G>A	GRCh38
NC_000023.10:g.66937352G>A , CM000685.1:g.66937352G>A	GRCh37
NC_000023.9:g.66854077G>A	NCBI36
NG_009014.2:g.178479G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*554G>A	ENSP00000379358.4:n.*554G>A
ENST00000374690.9:c.2206G>A MANE Select	ENSP00000363822.3:p.Ala736Thr
ENST00000396043.3:c.833G>A	ENSP00000379358.3:n.833G>A
ENST00000396044.8:c.2173+5821G>A	ENSP00000379359.3:n.2173+5821G>A
ENST00000612452.5:c.2206G>A	ENSP00000484033.2:p.Ala736Thr
ENST00000374690.7:c.2206G>A	ENSP00000363822.3:p.Ala736Thr
ENST00000396043.2:c.610G>A	ENSP00000379358.2:p.Ala204Thr
ENST00000396044.7:c.2173+5821G>A	ENSP00000379359.3:n.2173+5821G>A
ENST00000612452.4:c.1636G>A	ENSP00000484033.1:p.Ala546Thr
NM_000044.3:c.2206G>A	NP_000035.2:p.Ala736Thr
NM_001011645.2:c.610G>A	NP_001011645.1:p.Ala204Thr
NM_000044.4:c.2206G>A	NP_000035.2:p.Ala736Thr
NM_001011645.3:c.610G>A	NP_001011645.1:p.Ala204Thr
NM_000044.6:c.2206G>A MANE Select	NP_000035.2:p.Ala736Thr