Canonical Allele Identifier: CA16621466

Gene: AR

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721934G>A , CM000685.2:g.67721934G>A	GRCh38
NC_000023.10:g.66941776G>A , CM000685.1:g.66941776G>A	GRCh37
NC_000023.9:g.66858501G>A	NCBI36
NG_009014.2:g.182903G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*768G>A	ENSP00000379358.4:n.*768G>A
ENST00000374690.9:c.2420G>A MANE Select	ENSP00000363822.3:p.Cys807Tyr
ENST00000396043.3:c.1047G>A	ENSP00000379358.3:n.1047G>A
ENST00000396044.8:c.2174-1752G>A	ENSP00000379359.3:n.2174-1752G>A
ENST00000612452.5:c.2420G>A	ENSP00000484033.2:p.Cys807Tyr
ENST00000374690.7:c.2420G>A	ENSP00000363822.3:p.Cys807Tyr
ENST00000396043.2:c.824G>A	ENSP00000379358.2:p.Cys275Tyr
ENST00000396044.7:c.2174-1752G>A	ENSP00000379359.3:n.2174-1752G>A
ENST00000612452.4:c.1850G>A	ENSP00000484033.1:p.Cys617Tyr
NM_000044.3:c.2420G>A	NP_000035.2:p.Cys807Tyr
NM_001011645.2:c.824G>A	NP_001011645.1:p.Cys275Tyr
NM_000044.4:c.2420G>A	NP_000035.2:p.Cys807Tyr
NM_001011645.3:c.824G>A	NP_001011645.1:p.Cys275Tyr
NM_000044.6:c.2420G>A MANE Select	NP_000035.2:p.Cys807Tyr