Canonical Allele Identifier: CA413424295

Gene: AR

Linked Data

• dbSNP Id: rs749571801
• gnomAD v4: X-67717487-A-T
• MyVariant Identifiers: chrX:g.66937329A>T (hg19) ; chrX:g.67717487A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717487A>T , CM000685.2:g.67717487A>T	GRCh38
NC_000023.10:g.66937329A>T , CM000685.1:g.66937329A>T	GRCh37
NC_000023.9:g.66854054A>T	NCBI36
NG_009014.2:g.178456A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*531A>T	ENSP00000379358.4:n.*531A>T
ENST00000374690.9:c.2183A>T MANE Select	ENSP00000363822.3:p.Asn728Ile
ENST00000396043.3:c.810A>T	ENSP00000379358.3:n.810A>T
ENST00000396044.8:c.2173+5798A>T	ENSP00000379359.3:n.2173+5798A>T
ENST00000612452.5:c.2183A>T	ENSP00000484033.2:p.Asn728Ile
ENST00000374690.7:c.2183A>T	ENSP00000363822.3:p.Asn728Ile
ENST00000396043.2:c.587A>T	ENSP00000379358.2:p.Asn196Ile
ENST00000396044.7:c.2173+5798A>T	ENSP00000379359.3:n.2173+5798A>T
ENST00000612452.4:c.1613A>T	ENSP00000484033.1:p.Asn538Ile
NM_000044.3:c.2183A>T	NP_000035.2:p.Asn728Ile
NM_001011645.2:c.587A>T	NP_001011645.1:p.Asn196Ile
NM_000044.4:c.2183A>T	NP_000035.2:p.Asn728Ile
NM_001011645.3:c.587A>T	NP_001011645.1:p.Asn196Ile
NM_000044.6:c.2183A>T MANE Select	NP_000035.2:p.Asn728Ile