Canonical Allele Identifier: CA413423162

Gene: AR

Linked Data

• dbSNP Id: rs2147524500
• COSMIC: COSM5742318 ; COSM5742319 ; COSM5742320
• MyVariant Identifiers: chrX:g.66931343T>C (hg19) ; chrX:g.67711501T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711501T>C , CM000685.2:g.67711501T>C	GRCh38
NC_000023.10:g.66931343T>C , CM000685.1:g.66931343T>C	GRCh37
NC_000023.9:g.66848068T>C	NCBI36
NG_009014.2:g.172470T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*333T>C	ENSP00000379358.4:n.*333T>C
ENST00000374690.9:c.1985T>C MANE Select	ENSP00000363822.3:p.Val662Ala
ENST00000396043.3:c.612T>C	ENSP00000379358.3:n.612T>C
ENST00000396044.8:c.1985T>C	ENSP00000379359.3:p.Val662Ala
ENST00000612452.5:c.1985T>C	ENSP00000484033.2:p.Val662Ala
ENST00000374690.7:c.1985T>C	ENSP00000363822.3:p.Val662Ala
ENST00000396043.2:c.389T>C	ENSP00000379358.2:p.Val130Ala
ENST00000396044.7:c.1985T>C	ENSP00000379359.3:p.Val662Ala
ENST00000612452.4:c.1415T>C	ENSP00000484033.1:p.Val472Ala
NM_000044.3:c.1985T>C	NP_000035.2:p.Val662Ala
NM_001011645.2:c.389T>C	NP_001011645.1:p.Val130Ala
NM_000044.4:c.1985T>C	NP_000035.2:p.Val662Ala
NM_001011645.3:c.389T>C	NP_001011645.1:p.Val130Ala
NM_000044.6:c.1985T>C MANE Select	NP_000035.2:p.Val662Ala