Canonical Allele Identifier: CA10436628

Gene: AR

Linked Data

• dbSNP Id: rs761697885
• ExAC: X:66941703 A / G
• gnomAD v2: X-66941703-A-G
• gnomAD v3: X-67721861-A-G
• gnomAD v4: X-67721861-A-G
• MyVariant Identifiers: chrX:g.66941703A>G (hg19) ; chrX:g.67721861A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721861A>G , CM000685.2:g.67721861A>G	GRCh38
NC_000023.10:g.66941703A>G , CM000685.1:g.66941703A>G	GRCh37
NC_000023.9:g.66858428A>G	NCBI36
NG_009014.2:g.182830A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*695A>G	ENSP00000379358.4:n.*695A>G
ENST00000374690.9:c.2347A>G MANE Select	ENSP00000363822.3:p.Ser783Gly
ENST00000396043.3:c.974A>G	ENSP00000379358.3:n.974A>G
ENST00000396044.8:c.2174-1825A>G	ENSP00000379359.3:n.2174-1825A>G
ENST00000612452.5:c.2347A>G	ENSP00000484033.2:p.Ser783Gly
ENST00000374690.7:c.2347A>G	ENSP00000363822.3:p.Ser783Gly
ENST00000396043.2:c.751A>G	ENSP00000379358.2:p.Ser251Gly
ENST00000396044.7:c.2174-1825A>G	ENSP00000379359.3:n.2174-1825A>G
ENST00000612452.4:c.1777A>G	ENSP00000484033.1:p.Ser593Gly
NM_000044.3:c.2347A>G	NP_000035.2:p.Ser783Gly
NM_001011645.2:c.751A>G	NP_001011645.1:p.Ser251Gly
NM_000044.4:c.2347A>G	NP_000035.2:p.Ser783Gly
NM_001011645.3:c.751A>G	NP_001011645.1:p.Ser251Gly
NM_000044.6:c.2347A>G MANE Select	NP_000035.2:p.Ser783Gly