Canonical Allele Identifier: CA2435134820

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67722881A= , CM000685.2:g.67722881A=	GRCh38
NC_000023.10:g.66942723A= , CM000685.1:g.66942723A=	GRCh37
NC_000023.9:g.66859448A=	NCBI36
NG_009014.2:g.183850A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000044.6:c.2504A= MANE Select	NP_000035.2:p.Tyr835=
ENST00000374690.9:c.2504A= MANE Select	ENSP00000363822.3:p.Tyr835=
NM_000044.3:c.2504A=	NP_000035.2:p.Tyr835=
NM_000044.4:c.2504A=	NP_000035.2:p.Tyr835=
NM_001011645.2:c.908A=	NP_001011645.1:p.Tyr303=
NM_001011645.3:c.908A=	NP_001011645.1:p.Tyr303=
ENST00000374690.7:c.2504A=	ENSP00000363822.3:p.Tyr835=
ENST00000396043.2:c.908A=	ENSP00000379358.2:p.Tyr303=
ENST00000396043.3:c.1131A=	ENSP00000379358.3:n.1131A=
ENST00000396043.4:c.*852A=	ENSP00000379358.4:n.*852A=
ENST00000396044.7:c.2174-805A=	ENSP00000379359.3:n.2174-805A=
ENST00000396044.8:c.2174-805A=	ENSP00000379359.3:n.2174-805A=
ENST00000612452.4:c.1955A=	ENSP00000484033.1:p.Tyr652=
ENST00000612452.5:c.2504A=	ENSP00000484033.2:p.Tyr835=