Canonical Allele Identifier: CA517048195

Gene: AR

Linked Data

• MyVariant Identifiers: chrX:g.66931314C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711472C>T , CM000685.2:g.67711472C>T	GRCh38
NC_000023.10:g.66931314C>T , CM000685.1:g.66931314C>T	GRCh37
NC_000023.9:g.66848039C>T	NCBI36
NG_009014.2:g.172441C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*304C>T	ENSP00000379358.4:n.*304C>T
ENST00000374690.9:c.1956C>T MANE Select	ENSP00000363822.3:p.Pro652=
ENST00000396043.3:c.583C>T	ENSP00000379358.3:n.583C>T
ENST00000396044.8:c.1956C>T	ENSP00000379359.3:p.Pro652=
ENST00000612452.5:c.1956C>T	ENSP00000484033.2:p.Pro652=
ENST00000374690.7:c.1956C>T	ENSP00000363822.3:p.Pro652=
ENST00000396043.2:c.360C>T	ENSP00000379358.2:p.Pro120=
ENST00000396044.7:c.1956C>T	ENSP00000379359.3:p.Pro652=
ENST00000612452.4:c.1386C>T	ENSP00000484033.1:p.Pro462=
NM_000044.3:c.1956C>T	NP_000035.2:p.Pro652=
NM_001011645.2:c.360C>T	NP_001011645.1:p.Pro120=
NM_000044.4:c.1956C>T	NP_000035.2:p.Pro652=
NM_001011645.3:c.360C>T	NP_001011645.1:p.Pro120=
NM_000044.6:c.1956C>T MANE Select	NP_000035.2:p.Pro652=