Canonical Allele Identifier: CA413424670

Gene: AR

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717562G>A , CM000685.2:g.67717562G>A	GRCh38
NC_000023.10:g.66937404G>A , CM000685.1:g.66937404G>A	GRCh37
NC_000023.9:g.66854129G>A	NCBI36
NG_009014.2:g.178531G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*606G>A	ENSP00000379358.4:n.*606G>A
ENST00000374690.9:c.2258G>A MANE Select	ENSP00000363822.3:p.Arg753Gln
ENST00000396043.3:c.885G>A	ENSP00000379358.3:n.885G>A
ENST00000396044.8:c.2173+5873G>A	ENSP00000379359.3:n.2173+5873G>A
ENST00000612452.5:c.2258G>A	ENSP00000484033.2:p.Arg753Gln
ENST00000374690.7:c.2258G>A	ENSP00000363822.3:p.Arg753Gln
ENST00000396043.2:c.662G>A	ENSP00000379358.2:p.Arg221Gln
ENST00000396044.7:c.2173+5873G>A	ENSP00000379359.3:n.2173+5873G>A
ENST00000612452.4:c.1688G>A	ENSP00000484033.1:p.Arg563Gln
NM_000044.3:c.2258G>A	NP_000035.2:p.Arg753Gln
NM_001011645.2:c.662G>A	NP_001011645.1:p.Arg221Gln
NM_000044.4:c.2258G>A	NP_000035.2:p.Arg753Gln
NM_001011645.3:c.662G>A	NP_001011645.1:p.Arg221Gln
NM_000044.6:c.2258G>A MANE Select	NP_000035.2:p.Arg753Gln