Canonical Allele Identifier: CA2740092182

Gene: AR

Linked Data

• ClinVar Variation Id: 2951162
• ClinVar RCV Id: RCV003802424

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67722882del , CM000685.2:g.67722882del	GRCh38
NC_000023.10:g.66942724del , CM000685.1:g.66942724del	GRCh37
NC_000023.9:g.66859449del	NCBI36
NG_009014.2:g.183851del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*853del	ENSP00000379358.4:n.*853del
ENST00000374690.9:c.2505del MANE Select	ENSP00000363822.3:p.Tyr835Ter
ENST00000396043.3:c.1132del	ENSP00000379358.3:n.1132del
ENST00000396044.8:c.2174-804del	ENSP00000379359.3:n.2174-804del
ENST00000612452.5:c.2505del	ENSP00000484033.2:p.Tyr835Ter
ENST00000374690.7:c.2505del	ENSP00000363822.3:p.Tyr835Ter
ENST00000396043.2:c.909del	ENSP00000379358.2:p.Tyr303Ter
ENST00000396044.7:c.2174-804del	ENSP00000379359.3:n.2174-804del
ENST00000612452.4:c.1956del	ENSP00000484033.1:p.Tyr652Ter
NM_000044.3:c.2505del	NP_000035.2:p.Tyr835Ter
NM_001011645.2:c.909del	NP_001011645.1:p.Tyr303Ter
NM_000044.4:c.2505del	NP_000035.2:p.Tyr835Ter
NM_001011645.3:c.909del	NP_001011645.1:p.Tyr303Ter
NM_000044.6:c.2505del MANE Select	NP_000035.2:p.Tyr835Ter