Canonical Allele Identifier: CA413426837

Gene: AR

Linked Data

• dbSNP Id: rs2147535887
• gnomAD v4: X-67721915-A-G
• MyVariant Identifiers: chrX:g.66941757A>G (hg19) ; chrX:g.67721915A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721915A>G , CM000685.2:g.67721915A>G	GRCh38
NC_000023.10:g.66941757A>G , CM000685.1:g.66941757A>G	GRCh37
NC_000023.9:g.66858482A>G	NCBI36
NG_009014.2:g.182884A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*749A>G	ENSP00000379358.4:n.*749A>G
ENST00000374690.9:c.2401A>G MANE Select	ENSP00000363822.3:p.Thr801Ala
ENST00000396043.3:c.1028A>G	ENSP00000379358.3:n.1028A>G
ENST00000396044.8:c.2174-1771A>G	ENSP00000379359.3:n.2174-1771A>G
ENST00000612452.5:c.2401A>G	ENSP00000484033.2:p.Thr801Ala
ENST00000374690.7:c.2401A>G	ENSP00000363822.3:p.Thr801Ala
ENST00000396043.2:c.805A>G	ENSP00000379358.2:p.Thr269Ala
ENST00000396044.7:c.2174-1771A>G	ENSP00000379359.3:n.2174-1771A>G
ENST00000612452.4:c.1831A>G	ENSP00000484033.1:p.Thr611Ala
NM_000044.3:c.2401A>G	NP_000035.2:p.Thr801Ala
NM_001011645.2:c.805A>G	NP_001011645.1:p.Thr269Ala
NM_000044.4:c.2401A>G	NP_000035.2:p.Thr801Ala
NM_001011645.3:c.805A>G	NP_001011645.1:p.Thr269Ala
NM_000044.6:c.2401A>G MANE Select	NP_000035.2:p.Thr801Ala