Canonical Allele Identifier: CA2738703026

Gene: AR

Linked Data

• ClinVar Variation Id: 2931195
• ClinVar RCV Id: RCV003782457
• dbSNP Id: rs2147530500

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717465T>A , CM000685.2:g.67717465T>A	GRCh38
NC_000023.10:g.66937307T>A , CM000685.1:g.66937307T>A	GRCh37
NC_000023.9:g.66854032T>A	NCBI36
NG_009014.2:g.178434T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*522-13T>A	ENSP00000379358.4:n.*522-13T>A
ENST00000374690.9:c.2174-13T>A MANE Select	ENSP00000363822.3:n.2174-13T>A
ENST00000396043.3:c.801-13T>A	ENSP00000379358.3:n.801-13T>A
ENST00000396044.8:c.2173+5776T>A	ENSP00000379359.3:n.2173+5776T>A
ENST00000612452.5:c.2174-13T>A	ENSP00000484033.2:n.2174-13T>A
ENST00000374690.7:c.2174-13T>A	ENSP00000363822.3:n.2174-13T>A
ENST00000396043.2:c.578-13T>A	ENSP00000379358.2:n.578-13T>A
ENST00000396044.7:c.2173+5776T>A	ENSP00000379359.3:n.2173+5776T>A
ENST00000612452.4:c.1604-13T>A	ENSP00000484033.1:n.1604-13T>A
NM_000044.3:c.2174-13T>A	NP_000035.2:n.2174-13T>A
NM_001011645.2:c.578-13T>A	NP_001011645.1:n.578-13T>A
NM_000044.4:c.2174-13T>A	NP_000035.2:n.2174-13T>A
NM_001011645.3:c.578-13T>A	NP_001011645.1:n.578-13T>A
NM_000044.6:c.2174-13T>A MANE Select	NP_000035.2:n.2174-13T>A