Canonical Allele Identifier: CA413423057

Gene: AR

Linked Data

• dbSNP Id: rs2147524270
• MyVariant Identifiers: chrX:g.66931294G>A (hg19) ; chrX:g.67711452G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711452G>A , CM000685.2:g.67711452G>A	GRCh38
NC_000023.10:g.66931294G>A , CM000685.1:g.66931294G>A	GRCh37
NC_000023.9:g.66848019G>A	NCBI36
NG_009014.2:g.172421G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*284G>A	ENSP00000379358.4:n.*284G>A
ENST00000374690.9:c.1936G>A MANE Select	ENSP00000363822.3:p.Ala646Thr
ENST00000396043.3:c.563G>A	ENSP00000379358.3:n.563G>A
ENST00000396044.8:c.1936G>A	ENSP00000379359.3:p.Ala646Thr
ENST00000612452.5:c.1936G>A	ENSP00000484033.2:p.Ala646Thr
ENST00000374690.7:c.1936G>A	ENSP00000363822.3:p.Ala646Thr
ENST00000396043.2:c.340G>A	ENSP00000379358.2:p.Ala114Thr
ENST00000396044.7:c.1936G>A	ENSP00000379359.3:p.Ala646Thr
ENST00000612452.4:c.1366G>A	ENSP00000484033.1:p.Ala456Thr
NM_000044.3:c.1936G>A	NP_000035.2:p.Ala646Thr
NM_001011645.2:c.340G>A	NP_001011645.1:p.Ala114Thr
NM_000044.4:c.1936G>A	NP_000035.2:p.Ala646Thr
NM_001011645.3:c.340G>A	NP_001011645.1:p.Ala114Thr
NM_000044.6:c.1936G>A MANE Select	NP_000035.2:p.Ala646Thr