Canonical Allele Identifier: CA413424251

Gene: AR

Linked Data

• dbSNP Id: rs2147530554
• MyVariant Identifiers: chrX:g.66937320G>C (hg19) ; chrX:g.67717478G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717478G>C , CM000685.2:g.67717478G>C	GRCh38
NC_000023.10:g.66937320G>C , CM000685.1:g.66937320G>C	GRCh37
NC_000023.9:g.66854045G>C	NCBI36
NG_009014.2:g.178447G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*522G>C	ENSP00000379358.4:n.*522G>C
ENST00000374690.9:c.2174G>C MANE Select	ENSP00000363822.3:p.Gly725Ala
ENST00000396043.3:c.801G>C	ENSP00000379358.3:n.801G>C
ENST00000396044.8:c.2173+5789G>C	ENSP00000379359.3:n.2173+5789G>C
ENST00000612452.5:c.2174G>C	ENSP00000484033.2:p.Gly725Ala
ENST00000374690.7:c.2174G>C	ENSP00000363822.3:p.Gly725Ala
ENST00000396043.2:c.578G>C	ENSP00000379358.2:p.Gly193Ala
ENST00000396044.7:c.2173+5789G>C	ENSP00000379359.3:n.2173+5789G>C
ENST00000612452.4:c.1604G>C	ENSP00000484033.1:p.Gly535Ala
NM_000044.3:c.2174G>C	NP_000035.2:p.Gly725Ala
NM_001011645.2:c.578G>C	NP_001011645.1:p.Gly193Ala
NM_000044.4:c.2174G>C	NP_000035.2:p.Gly725Ala
NM_001011645.3:c.578G>C	NP_001011645.1:p.Gly193Ala
NM_000044.6:c.2174G>C MANE Select	NP_000035.2:p.Gly725Ala