Canonical Allele Identifier: CA413424776

Gene: AR

Linked Data

• dbSNP Id: rs2147531141
• MyVariant Identifiers: chrX:g.66937449A>T (hg19) ; chrX:g.67717607A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717607A>T , CM000685.2:g.67717607A>T	GRCh38
NC_000023.10:g.66937449A>T , CM000685.1:g.66937449A>T	GRCh37
NC_000023.9:g.66854174A>T	NCBI36
NG_009014.2:g.178576A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*651A>T	ENSP00000379358.4:n.*651A>T
ENST00000374690.9:c.2303A>T MANE Select	ENSP00000363822.3:p.Asp768Val
ENST00000396043.3:c.930A>T	ENSP00000379358.3:n.930A>T
ENST00000396044.8:c.2173+5918A>T	ENSP00000379359.3:n.2173+5918A>T
ENST00000612452.5:c.2303A>T	ENSP00000484033.2:p.Asp768Val
ENST00000374690.7:c.2303A>T	ENSP00000363822.3:p.Asp768Val
ENST00000396043.2:c.707A>T	ENSP00000379358.2:p.Asp236Val
ENST00000396044.7:c.2173+5918A>T	ENSP00000379359.3:n.2173+5918A>T
ENST00000612452.4:c.1733A>T	ENSP00000484033.1:p.Asp578Val
NM_000044.3:c.2303A>T	NP_000035.2:p.Asp768Val
NM_001011645.2:c.707A>T	NP_001011645.1:p.Asp236Val
NM_000044.4:c.2303A>T	NP_000035.2:p.Asp768Val
NM_001011645.3:c.707A>T	NP_001011645.1:p.Asp236Val
NM_000044.6:c.2303A>T MANE Select	NP_000035.2:p.Asp768Val