Canonical Allele Identifier: CA2580101282

Gene: AR

Linked Data

• ClinVar Variation Id: 2016344
• ClinVar RCV Id: RCV002851524

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717495_67717503del , CM000685.2:g.67717495_67717503del	GRCh38
NC_000023.10:g.66937337_66937345del , CM000685.1:g.66937337_66937345del	GRCh37
NC_000023.9:g.66854062_66854070del	NCBI36
NG_009014.2:g.178464_178472del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*539_*547del	ENSP00000379358.4:n.*539_*547del
ENST00000374690.9:c.2191_2199del MANE Select	ENSP00000363822.3:p.Val731_Asp733del
ENST00000396043.3:c.818_826del	ENSP00000379358.3:n.818_826del
ENST00000396044.8:c.2173+5806_2173+5814del	ENSP00000379359.3:n.2173+5806_2173+5814del
ENST00000612452.5:c.2191_2199del	ENSP00000484033.2:p.Val731_Asp733del
ENST00000374690.7:c.2191_2199del	ENSP00000363822.3:p.Val731_Asp733del
ENST00000396043.2:c.595_603del	ENSP00000379358.2:p.Val199_Asp201del
ENST00000396044.7:c.2173+5806_2173+5814del	ENSP00000379359.3:n.2173+5806_2173+5814del
ENST00000612452.4:c.1621_1629del	ENSP00000484033.1:p.Val541_Asp543del
NM_000044.3:c.2191_2199del	NP_000035.2:p.Val731_Asp733del
NM_001011645.2:c.595_603del	NP_001011645.1:p.Val199_Asp201del
NM_000044.4:c.2191_2199del	NP_000035.2:p.Val731_Asp733del
NM_001011645.3:c.595_603del	NP_001011645.1:p.Val199_Asp201del
NM_000044.6:c.2191_2199del MANE Select	NP_000035.2:p.Val731_Asp733del