Canonical Allele Identifier: CA413423329

Gene: AR

Linked Data

• dbSNP Id: rs2147524871
• gnomAD v4: X-67711578-G-T
• MyVariant Identifiers: chrX:g.66931420G>T (hg19) ; chrX:g.67711578G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711578G>T , CM000685.2:g.67711578G>T	GRCh38
NC_000023.10:g.66931420G>T , CM000685.1:g.66931420G>T	GRCh37
NC_000023.9:g.66848145G>T	NCBI36
NG_009014.2:g.172547G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*410G>T	ENSP00000379358.4:n.*410G>T
ENST00000374690.9:c.2062G>T MANE Select	ENSP00000363822.3:p.Ala688Ser
ENST00000396043.3:c.689G>T	ENSP00000379358.3:n.689G>T
ENST00000396044.8:c.2062G>T	ENSP00000379359.3:p.Ala688Ser
ENST00000612452.5:c.2062G>T	ENSP00000484033.2:p.Ala688Ser
ENST00000374690.7:c.2062G>T	ENSP00000363822.3:p.Ala688Ser
ENST00000396043.2:c.466G>T	ENSP00000379358.2:p.Ala156Ser
ENST00000396044.7:c.2062G>T	ENSP00000379359.3:p.Ala688Ser
ENST00000612452.4:c.1492G>T	ENSP00000484033.1:p.Ala498Ser
NM_000044.3:c.2062G>T	NP_000035.2:p.Ala688Ser
NM_001011645.2:c.466G>T	NP_001011645.1:p.Ala156Ser
NM_000044.4:c.2062G>T	NP_000035.2:p.Ala688Ser
NM_001011645.3:c.466G>T	NP_001011645.1:p.Ala156Ser
NM_000044.6:c.2062G>T MANE Select	NP_000035.2:p.Ala688Ser