Canonical Allele Identifier: CA413428273

Gene: AR

Linked Data

• dbSNP Id: rs2147540423
• MyVariant Identifiers: chrX:g.66943583T>A (hg19) ; chrX:g.67723741T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67723741T>A , CM000685.2:g.67723741T>A	GRCh38
NC_000023.10:g.66943583T>A , CM000685.1:g.66943583T>A	GRCh37
NC_000023.9:g.66860308T>A	NCBI36
NG_009014.2:g.184710T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*1011T>A	ENSP00000379358.4:n.*1011T>A
ENST00000374690.9:c.2663T>A MANE Select	ENSP00000363822.3:p.Val888Glu
ENST00000396043.3:c.1290T>A	ENSP00000379358.3:n.1290T>A
ENST00000396044.8:c.*24T>A	ENSP00000379359.3:n.*24T>A
ENST00000612452.5:c.2663T>A	ENSP00000484033.2:p.Val888Glu
ENST00000374690.7:c.2663T>A	ENSP00000363822.3:p.Val888Glu
ENST00000396043.2:c.1067T>A	ENSP00000379358.2:p.Val356Glu
ENST00000396044.7:c.*24T>A	ENSP00000379359.3:n.*24T>A
ENST00000612452.4:c.2114T>A	ENSP00000484033.1:p.Val705Glu
NM_000044.3:c.2663T>A	NP_000035.2:p.Val888Glu
NM_001011645.2:c.1067T>A	NP_001011645.1:p.Val356Glu
NM_000044.4:c.2663T>A	NP_000035.2:p.Val888Glu
NM_001011645.3:c.1067T>A	NP_001011645.1:p.Val356Glu
NM_000044.6:c.2663T>A MANE Select	NP_000035.2:p.Val888Glu