Canonical Allele Identifier: CA413423061

Gene: AR

Linked Data

• dbSNP Id: rs1800053
• MyVariant Identifiers: chrX:g.66931295C>T (hg19) ; chrX:g.67711453C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711453C>T , CM000685.2:g.67711453C>T	GRCh38
NC_000023.10:g.66931295C>T , CM000685.1:g.66931295C>T	GRCh37
NC_000023.9:g.66848020C>T	NCBI36
NG_009014.2:g.172422C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*285C>T	ENSP00000379358.4:n.*285C>T
ENST00000374690.9:c.1937C>T MANE Select	ENSP00000363822.3:p.Ala646Val
ENST00000396043.3:c.564C>T	ENSP00000379358.3:n.564C>T
ENST00000396044.8:c.1937C>T	ENSP00000379359.3:p.Ala646Val
ENST00000612452.5:c.1937C>T	ENSP00000484033.2:p.Ala646Val
ENST00000374690.7:c.1937C>T	ENSP00000363822.3:p.Ala646Val
ENST00000396043.2:c.341C>T	ENSP00000379358.2:p.Ala114Val
ENST00000396044.7:c.1937C>T	ENSP00000379359.3:p.Ala646Val
ENST00000612452.4:c.1367C>T	ENSP00000484033.1:p.Ala456Val
NM_000044.3:c.1937C>T	NP_000035.2:p.Ala646Val
NM_001011645.2:c.341C>T	NP_001011645.1:p.Ala114Val
NM_000044.4:c.1937C>T	NP_000035.2:p.Ala646Val
NM_001011645.3:c.341C>T	NP_001011645.1:p.Ala114Val
NM_000044.6:c.1937C>T MANE Select	NP_000035.2:p.Ala646Val