Canonical Allele Identifier: CA413426805

Gene: AR

Linked Data

• dbSNP Id: rs2147535873
• MyVariant Identifiers: chrX:g.66941752A>T (hg19) ; chrX:g.67721910A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721910A>T , CM000685.2:g.67721910A>T	GRCh38
NC_000023.10:g.66941752A>T , CM000685.1:g.66941752A>T	GRCh37
NC_000023.9:g.66858477A>T	NCBI36
NG_009014.2:g.182879A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*744A>T	ENSP00000379358.4:n.*744A>T
ENST00000374690.9:c.2396A>T MANE Select	ENSP00000363822.3:p.Gln799Leu
ENST00000396043.3:c.1023A>T	ENSP00000379358.3:n.1023A>T
ENST00000396044.8:c.2174-1776A>T	ENSP00000379359.3:n.2174-1776A>T
ENST00000612452.5:c.2396A>T	ENSP00000484033.2:p.Gln799Leu
ENST00000374690.7:c.2396A>T	ENSP00000363822.3:p.Gln799Leu
ENST00000396043.2:c.800A>T	ENSP00000379358.2:p.Gln267Leu
ENST00000396044.7:c.2174-1776A>T	ENSP00000379359.3:n.2174-1776A>T
ENST00000612452.4:c.1826A>T	ENSP00000484033.1:p.Gln609Leu
NM_000044.3:c.2396A>T	NP_000035.2:p.Gln799Leu
NM_001011645.2:c.800A>T	NP_001011645.1:p.Gln267Leu
NM_000044.4:c.2396A>T	NP_000035.2:p.Gln799Leu
NM_001011645.3:c.800A>T	NP_001011645.1:p.Gln267Leu
NM_000044.6:c.2396A>T MANE Select	NP_000035.2:p.Gln799Leu