Canonical Allele Identifier: CA2435119882

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67686104T= , CM000685.2:g.67686104T=	GRCh38
NC_000023.10:g.66905946T= , CM000685.1:g.66905946T=	GRCh37
NC_000023.9:g.66822671T=	NCBI36
NG_009014.2:g.147073T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*211T=	ENSP00000379358.4:n.*211T=
ENST00000374690.9:c.1863T= MANE Select	ENSP00000363822.3:p.Tyr621=
ENST00000396043.3:c.490T=	ENSP00000379358.3:n.490T=
ENST00000396044.8:c.1863T=	ENSP00000379359.3:p.Tyr621=
ENST00000612452.5:c.1863T=	ENSP00000484033.2:p.Tyr621=
ENST00000374690.7:c.1863T=	ENSP00000363822.3:p.Tyr621=
ENST00000396043.2:c.267T=	ENSP00000379358.2:p.Tyr89=
ENST00000396044.7:c.1863T=	ENSP00000379359.3:p.Tyr621=
ENST00000504326.5:c.1863T=	ENSP00000421155.1:p.Tyr621=
ENST00000513847.5:n.2190T=
ENST00000514029.5:c.*344T=	ENSP00000425199.1:n.*344T=
ENST00000612010.4:c.*215T=	ENSP00000482407.1:n.*215T=
ENST00000612452.4:c.1293T=	ENSP00000484033.1:p.Tyr431=
ENST00000613054.2:c.*61T=	ENSP00000479013.1:n.*61T=
NM_000044.3:c.1863T=	NP_000035.2:p.Tyr621=
NM_001011645.2:c.267T=	NP_001011645.1:p.Tyr89=
NM_000044.4:c.1863T=	NP_000035.2:p.Tyr621=
NM_001011645.3:c.267T=	NP_001011645.1:p.Tyr89=
NM_001348061.1:c.1863T=	NP_001334990.1:p.Tyr621=
NM_001348063.1:c.1863T=	NP_001334992.1:p.Tyr621=
NM_001348064.1:c.*61T=	NP_001334993.1:n.*61T=
NM_000044.6:c.1863T= MANE Select	NP_000035.2:p.Tyr621=