Canonical Allele Identifier: CA120752

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711680G>A , CM000685.2:g.67711680G>A	GRCh38
NC_000023.10:g.66931522G>A , CM000685.1:g.66931522G>A	GRCh37
NC_000023.9:g.66848247G>A	NCBI36
NG_009014.2:g.172649G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000044.6:c.2164G>A MANE Select	NP_000035.2:p.Ala722Thr
ENST00000374690.9:c.2164G>A MANE Select	ENSP00000363822.3:p.Ala722Thr
NM_000044.3:c.2164G>A	NP_000035.2:p.Ala722Thr
NM_000044.4:c.2164G>A	NP_000035.2:p.Ala722Thr
NM_001011645.2:c.568G>A	NP_001011645.1:p.Ala190Thr
NM_001011645.3:c.568G>A	NP_001011645.1:p.Ala190Thr
ENST00000374690.7:c.2164G>A	ENSP00000363822.3:p.Ala722Thr
ENST00000396043.2:c.568G>A	ENSP00000379358.2:p.Ala190Thr
ENST00000396043.3:c.791G>A	ENSP00000379358.3:n.791G>A
ENST00000396043.4:c.*512G>A	ENSP00000379358.4:n.*512G>A
ENST00000396044.7:c.2164G>A	ENSP00000379359.3:p.Ala722Thr
ENST00000396044.8:c.2164G>A	ENSP00000379359.3:p.Ala722Thr
ENST00000612452.4:c.1594G>A	ENSP00000484033.1:p.Ala532Thr
ENST00000612452.5:c.2164G>A	ENSP00000484033.2:p.Ala722Thr