Canonical Allele Identifier: CA517048358

Gene: AR

Linked Data

• dbSNP Id: rs2147524765
• MyVariant Identifiers: chrX:g.66931401T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711559T>A , CM000685.2:g.67711559T>A	GRCh38
NC_000023.10:g.66931401T>A , CM000685.1:g.66931401T>A	GRCh37
NC_000023.9:g.66848126T>A	NCBI36
NG_009014.2:g.172528T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*391T>A	ENSP00000379358.4:n.*391T>A
ENST00000374690.9:c.2043T>A MANE Select	ENSP00000363822.3:p.Ile681=
ENST00000396043.3:c.670T>A	ENSP00000379358.3:n.670T>A
ENST00000396044.8:c.2043T>A	ENSP00000379359.3:p.Ile681=
ENST00000612452.5:c.2043T>A	ENSP00000484033.2:p.Ile681=
ENST00000374690.7:c.2043T>A	ENSP00000363822.3:p.Ile681=
ENST00000396043.2:c.447T>A	ENSP00000379358.2:p.Ile149=
ENST00000396044.7:c.2043T>A	ENSP00000379359.3:p.Ile681=
ENST00000612452.4:c.1473T>A	ENSP00000484033.1:p.Ile491=
NM_000044.3:c.2043T>A	NP_000035.2:p.Ile681=
NM_001011645.2:c.447T>A	NP_001011645.1:p.Ile149=
NM_000044.4:c.2043T>A	NP_000035.2:p.Ile681=
NM_001011645.3:c.447T>A	NP_001011645.1:p.Ile149=
NM_000044.6:c.2043T>A MANE Select	NP_000035.2:p.Ile681=