Canonical Allele Identifier: CA952600192

Gene: ANAPC5

Linked Data

• dbSNP Id: rs1902464213
• gnomAD v3: 12-121318576-AT-A
• gnomAD v4: 12-121318576-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121318579del , CM000674.2:g.121318579del	GRCh38
NC_000012.11:g.121756382del , CM000674.1:g.121756382del	GRCh37
NC_000012.10:g.120240765del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261819.8:c.1669del MANE Select	ENSP00000261819.3:p.Met557CysfsTer18
ENST00000261819.7:c.1669del	ENSP00000261819.3:p.Met557CysfsTer18
ENST00000366333.3:n.881del
ENST00000441917.6:c.1333del	ENSP00000415061.2:p.Met445CysfsTer18
ENST00000534976.5:n.2325del
ENST00000535482.1:c.667del	ENSP00000438754.1:p.Met223CysfsTer18
ENST00000535641.5:n.1880del
ENST00000539079.5:c.1013del
ENST00000541887.5:c.1630del	ENSP00000439875.1:p.Met544CysfsTer18
ENST00000544314.5:n.787del
ENST00000545218.5:n.912del
NM_001137559.1:c.1333del	NP_001131031.1:p.Met445CysfsTer18
NM_016237.4:c.1669del	NP_057321.2:p.Met557CysfsTer18
XM_005253900.2:c.1630del	XP_005253957.1:p.Met544CysfsTer18
XM_006719449.1:c.475del	XP_006719512.1:p.Met159CysfsTer18
NM_001330489.1:c.1630del	NP_001317418.1:p.Met544CysfsTer18
XM_017019423.2:c.475del	XP_016874912.1:p.Met159CysfsTer18
XM_017019424.2:c.475del	XP_016874913.1:p.Met159CysfsTer18
NM_016237.5:c.1669del MANE Select	NP_057321.2:p.Met557CysfsTer18
NM_001330489.2:c.1630del	NP_001317418.1:p.Met544CysfsTer18