Canonical Allele Identifier: CA413428176

Gene: AR

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67723701C>G , CM000685.2:g.67723701C>G	GRCh38
NC_000023.10:g.66943543C>G , CM000685.1:g.66943543C>G	GRCh37
NC_000023.9:g.66860268C>G	NCBI36
NG_009014.2:g.184670C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*971C>G	ENSP00000379358.4:n.*971C>G
ENST00000374690.9:c.2623C>G MANE Select	ENSP00000363822.3:p.His875Asp
ENST00000396043.3:c.1250C>G	ENSP00000379358.3:n.1250C>G
ENST00000396044.8:c.2189C>G	ENSP00000379359.3:p.Ala730Gly
ENST00000612452.5:c.2623C>G	ENSP00000484033.2:p.His875Asp
ENST00000374690.7:c.2623C>G	ENSP00000363822.3:p.His875Asp
ENST00000396043.2:c.1027C>G	ENSP00000379358.2:p.His343Asp
ENST00000396044.7:c.2189C>G	ENSP00000379359.3:p.Ala730Gly
ENST00000612452.4:c.2074C>G	ENSP00000484033.1:p.His692Asp
NM_000044.3:c.2623C>G	NP_000035.2:p.His875Asp
NM_001011645.2:c.1027C>G	NP_001011645.1:p.His343Asp
NM_000044.4:c.2623C>G	NP_000035.2:p.His875Asp
NM_001011645.3:c.1027C>G	NP_001011645.1:p.His343Asp
NM_000044.6:c.2623C>G MANE Select	NP_000035.2:p.His875Asp