Canonical Allele Identifier: CA2580101276

Gene: AR

Linked Data

• ClinVar Variation Id: 2430349
• ClinVar RCV Id: RCV003128527

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721898_67721899del , CM000685.2:g.67721898_67721899del	GRCh38
NC_000023.10:g.66941740_66941741del , CM000685.1:g.66941740_66941741del	GRCh37
NC_000023.9:g.66858465_66858466del	NCBI36
NG_009014.2:g.182867_182868del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*732_*733del	ENSP00000379358.4:n.*732_*733del
ENST00000374690.9:c.2384_2385del MANE Select	ENSP00000363822.3:p.Phe795TrpfsTer?
ENST00000396043.3:c.1011_1012del	ENSP00000379358.3:n.1011_1012del
ENST00000396044.8:c.2174-1788_2174-1787del	ENSP00000379359.3:n.2174-1788_2174-1787del
ENST00000612452.5:c.2384_2385del	ENSP00000484033.2:p.Phe795TrpfsTer?
ENST00000374690.7:c.2384_2385del	ENSP00000363822.3:p.Phe795TrpfsTer?
ENST00000396043.2:c.788_789del	ENSP00000379358.2:p.Phe263TrpfsTer?
ENST00000396044.7:c.2174-1788_2174-1787del	ENSP00000379359.3:n.2174-1788_2174-1787del
ENST00000612452.4:c.1814_1815del	ENSP00000484033.1:p.Phe605TrpfsTer22
NM_000044.3:c.2384_2385del	NP_000035.2:p.Phe795TrpfsTer?
NM_001011645.2:c.788_789del	NP_001011645.1:p.Phe263TrpfsTer?
NM_000044.4:c.2384_2385del	NP_000035.2:p.Phe795TrpfsTer?
NM_001011645.3:c.788_789del	NP_001011645.1:p.Phe263TrpfsTer?
NM_000044.6:c.2384_2385del MANE Select	NP_000035.2:p.Phe795TrpfsTer?