Canonical Allele Identifier: CA413427992

Gene: AR

Linked Data

• MyVariant Identifiers: chrX:g.66942764A>C (hg19) ; chrX:g.67722922A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67722922A>C , CM000685.2:g.67722922A>C	GRCh38
NC_000023.10:g.66942764A>C , CM000685.1:g.66942764A>C	GRCh37
NC_000023.9:g.66859489A>C	NCBI36
NG_009014.2:g.183891A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*893A>C	ENSP00000379358.4:n.*893A>C
ENST00000374690.9:c.2545A>C MANE Select	ENSP00000363822.3:p.Asn849His
ENST00000396043.3:c.1172A>C	ENSP00000379358.3:n.1172A>C
ENST00000396044.8:c.2174-764A>C	ENSP00000379359.3:n.2174-764A>C
ENST00000612452.5:c.2545A>C	ENSP00000484033.2:p.Asn849His
ENST00000374690.7:c.2545A>C	ENSP00000363822.3:p.Asn849His
ENST00000396043.2:c.949A>C	ENSP00000379358.2:p.Asn317His
ENST00000396044.7:c.2174-764A>C	ENSP00000379359.3:n.2174-764A>C
ENST00000612452.4:c.1996A>C	ENSP00000484033.1:p.Asn666His
NM_000044.3:c.2545A>C	NP_000035.2:p.Asn849His
NM_001011645.2:c.949A>C	NP_001011645.1:p.Asn317His
NM_000044.4:c.2545A>C	NP_000035.2:p.Asn849His
NM_001011645.3:c.949A>C	NP_001011645.1:p.Asn317His
NM_000044.6:c.2545A>C MANE Select	NP_000035.2:p.Asn849His