Canonical Allele Identifier: CA16608973

Gene: AR

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711653C>A , CM000685.2:g.67711653C>A	GRCh38
NC_000023.10:g.66931495C>A , CM000685.1:g.66931495C>A	GRCh37
NC_000023.9:g.66848220C>A	NCBI36
NG_009014.2:g.172622C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*485C>A	ENSP00000379358.4:n.*485C>A
ENST00000374690.9:c.2137C>A MANE Select	ENSP00000363822.3:p.Leu713Ile
ENST00000396043.3:c.764C>A	ENSP00000379358.3:n.764C>A
ENST00000396044.8:c.2137C>A	ENSP00000379359.3:p.Leu713Ile
ENST00000612452.5:c.2137C>A	ENSP00000484033.2:p.Leu713Ile
ENST00000374690.7:c.2137C>A	ENSP00000363822.3:p.Leu713Ile
ENST00000396043.2:c.541C>A	ENSP00000379358.2:p.Leu181Ile
ENST00000396044.7:c.2137C>A	ENSP00000379359.3:p.Leu713Ile
ENST00000612452.4:c.1567C>A	ENSP00000484033.1:p.Leu523Ile
NM_000044.3:c.2137C>A	NP_000035.2:p.Leu713Ile
NM_001011645.2:c.541C>A	NP_001011645.1:p.Leu181Ile
NM_000044.4:c.2137C>A	NP_000035.2:p.Leu713Ile
NM_001011645.3:c.541C>A	NP_001011645.1:p.Leu181Ile
NM_000044.6:c.2137C>A MANE Select	NP_000035.2:p.Leu713Ile