Canonical Allele Identifier: CA2435134328

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721848G= , CM000685.2:g.67721848G=	GRCh38
NC_000023.10:g.66941690G= , CM000685.1:g.66941690G=	GRCh37
NC_000023.9:g.66858415G=	NCBI36
NG_009014.2:g.182817G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*682G=	ENSP00000379358.4:n.*682G=
ENST00000374690.9:c.2334G= MANE Select	ENSP00000363822.3:p.Lys778=
ENST00000396043.3:c.961G=	ENSP00000379358.3:n.961G=
ENST00000396044.8:c.2174-1838G=	ENSP00000379359.3:n.2174-1838G=
ENST00000612452.5:c.2334G=	ENSP00000484033.2:p.Lys778=
ENST00000374690.7:c.2334G=	ENSP00000363822.3:p.Lys778=
ENST00000396043.2:c.738G=	ENSP00000379358.2:p.Lys246=
ENST00000396044.7:c.2174-1838G=	ENSP00000379359.3:n.2174-1838G=
ENST00000612452.4:c.1764G=	ENSP00000484033.1:p.Lys588=
NM_000044.3:c.2334G=	NP_000035.2:p.Lys778=
NM_001011645.2:c.738G=	NP_001011645.1:p.Lys246=
NM_000044.4:c.2334G=	NP_000035.2:p.Lys778=
NM_001011645.3:c.738G=	NP_001011645.1:p.Lys246=
NM_000044.6:c.2334G= MANE Select	NP_000035.2:p.Lys778=