Canonical Allele Identifier: CA413428282

Gene: AR

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67723745C>G , CM000685.2:g.67723745C>G	GRCh38
NC_000023.10:g.66943587C>G , CM000685.1:g.66943587C>G	GRCh37
NC_000023.9:g.66860312C>G	NCBI36
NG_009014.2:g.184714C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*1015C>G	ENSP00000379358.4:n.*1015C>G
ENST00000374690.9:c.2667C>G MANE Select	ENSP00000363822.3:p.Ser889Arg
ENST00000396043.3:c.1294C>G	ENSP00000379358.3:n.1294C>G
ENST00000396044.8:c.*28C>G	ENSP00000379359.3:n.*28C>G
ENST00000612452.5:c.2667C>G	ENSP00000484033.2:p.Ser889Arg
ENST00000374690.7:c.2667C>G	ENSP00000363822.3:p.Ser889Arg
ENST00000396043.2:c.1071C>G	ENSP00000379358.2:p.Ser357Arg
ENST00000396044.7:c.*28C>G	ENSP00000379359.3:n.*28C>G
ENST00000612452.4:c.2118C>G	ENSP00000484033.1:p.Ser706Arg
NM_000044.3:c.2667C>G	NP_000035.2:p.Ser889Arg
NM_001011645.2:c.1071C>G	NP_001011645.1:p.Ser357Arg
NM_000044.4:c.2667C>G	NP_000035.2:p.Ser889Arg
NM_001011645.3:c.1071C>G	NP_001011645.1:p.Ser357Arg
NM_000044.6:c.2667C>G MANE Select	NP_000035.2:p.Ser889Arg