Canonical Allele Identifier: CA413423559

Gene: AR

Linked Data

• dbSNP Id: rs2147525349
• MyVariant Identifiers: chrX:g.66931525T>G (hg19) ; chrX:g.67711683T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711683T>G , CM000685.2:g.67711683T>G	GRCh38
NC_000023.10:g.66931525T>G , CM000685.1:g.66931525T>G	GRCh37
NC_000023.9:g.66848250T>G	NCBI36
NG_009014.2:g.172652T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*515T>G	ENSP00000379358.4:n.*515T>G
ENST00000374690.9:c.2167T>G MANE Select	ENSP00000363822.3:p.Leu723Val
ENST00000396043.3:c.794T>G	ENSP00000379358.3:n.794T>G
ENST00000396044.8:c.2167T>G	ENSP00000379359.3:p.Leu723Val
ENST00000612452.5:c.2167T>G	ENSP00000484033.2:p.Leu723Val
ENST00000374690.7:c.2167T>G	ENSP00000363822.3:p.Leu723Val
ENST00000396043.2:c.571T>G	ENSP00000379358.2:p.Leu191Val
ENST00000396044.7:c.2167T>G	ENSP00000379359.3:p.Leu723Val
ENST00000612452.4:c.1597T>G	ENSP00000484033.1:p.Leu533Val
NM_000044.3:c.2167T>G	NP_000035.2:p.Leu723Val
NM_001011645.2:c.571T>G	NP_001011645.1:p.Leu191Val
NM_000044.4:c.2167T>G	NP_000035.2:p.Leu723Val
NM_001011645.3:c.571T>G	NP_001011645.1:p.Leu191Val
NM_000044.6:c.2167T>G MANE Select	NP_000035.2:p.Leu723Val