Canonical Allele Identifier: CA330772299

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67722905T>C , CM000685.2:g.67722905T>C	GRCh38
NC_000023.10:g.66942747T>C , CM000685.1:g.66942747T>C	GRCh37
NC_000023.9:g.66859472T>C	NCBI36
NG_009014.2:g.183874T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000044.6:c.2528T>C MANE Select	NP_000035.2:p.Ile843Thr
ENST00000374690.9:c.2528T>C MANE Select	ENSP00000363822.3:p.Ile843Thr
NM_000044.3:c.2528T>C	NP_000035.2:p.Ile843Thr
NM_000044.4:c.2528T>C	NP_000035.2:p.Ile843Thr
NM_001011645.2:c.932T>C	NP_001011645.1:p.Ile311Thr
NM_001011645.3:c.932T>C	NP_001011645.1:p.Ile311Thr
ENST00000374690.7:c.2528T>C	ENSP00000363822.3:p.Ile843Thr
ENST00000396043.2:c.932T>C	ENSP00000379358.2:p.Ile311Thr
ENST00000396043.3:c.1155T>C	ENSP00000379358.3:n.1155T>C
ENST00000396043.4:c.*876T>C	ENSP00000379358.4:n.*876T>C
ENST00000396044.7:c.2174-781T>C	ENSP00000379359.3:n.2174-781T>C
ENST00000396044.8:c.2174-781T>C	ENSP00000379359.3:n.2174-781T>C
ENST00000612452.4:c.1979T>C	ENSP00000484033.1:p.Ile660Thr
ENST00000612452.5:c.2528T>C	ENSP00000484033.2:p.Ile843Thr