Canonical Allele Identifier: CA2435132651

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717552A= , CM000685.2:g.67717552A=	GRCh38
NC_000023.10:g.66937394A= , CM000685.1:g.66937394A=	GRCh37
NC_000023.9:g.66854119A=	NCBI36
NG_009014.2:g.178521A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000044.6:c.2248A= MANE Select	NP_000035.2:p.Met750=
ENST00000374690.9:c.2248A= MANE Select	ENSP00000363822.3:p.Met750=
NM_000044.3:c.2248A=	NP_000035.2:p.Met750=
NM_000044.4:c.2248A=	NP_000035.2:p.Met750=
NM_001011645.2:c.652A=	NP_001011645.1:p.Met218=
NM_001011645.3:c.652A=	NP_001011645.1:p.Met218=
ENST00000374690.7:c.2248A=	ENSP00000363822.3:p.Met750=
ENST00000396043.2:c.652A=	ENSP00000379358.2:p.Met218=
ENST00000396043.3:c.875A=	ENSP00000379358.3:n.875A=
ENST00000396043.4:c.*596A=	ENSP00000379358.4:n.*596A=
ENST00000396044.7:c.2173+5863A=	ENSP00000379359.3:n.2173+5863A=
ENST00000396044.8:c.2173+5863A=	ENSP00000379359.3:n.2173+5863A=
ENST00000612452.4:c.1678A=	ENSP00000484033.1:p.Met560=
ENST00000612452.5:c.2248A=	ENSP00000484033.2:p.Met750=