Canonical Allele Identifier: CA2621415576

Gene: ANAPC5

Linked Data

• gnomAD v4: 12-121318432-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121318435del , CM000674.2:g.121318435del	GRCh38
NC_000012.11:g.121756238del , CM000674.1:g.121756238del	GRCh37
NC_000012.10:g.120240621del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261819.8:c.1746-9del MANE Select	ENSP00000261819.3:n.1746-9del
ENST00000261819.7:c.1746-9del	ENSP00000261819.3:n.1746-9del
ENST00000441917.6:c.1410-9del	ENSP00000415061.2:n.1410-9del
ENST00000534976.5:n.2469del
ENST00000535482.1:c.744-9del	ENSP00000438754.1:n.744-9del
ENST00000535641.5:n.1957-9del
ENST00000539079.5:c.1090-29del
ENST00000541887.5:c.1707-9del	ENSP00000439875.1:n.1707-9del
ENST00000544314.5:n.864-9del
ENST00000545218.5:n.988+68del
NM_001137559.1:c.1410-9del	NP_001131031.1:n.1410-9del
NM_016237.4:c.1746-9del	NP_057321.2:n.1746-9del
XM_005253900.2:c.1707-9del	XP_005253957.1:n.1707-9del
XM_006719449.1:c.552-9del	XP_006719512.1:n.552-9del
NM_001330489.1:c.1707-9del	NP_001317418.1:n.1707-9del
XM_017019423.2:c.552-9del	XP_016874912.1:n.552-9del
XM_017019424.2:c.552-9del	XP_016874913.1:n.552-9del
NM_016237.5:c.1746-9del MANE Select	NP_057321.2:n.1746-9del
NM_001330489.2:c.1707-9del	NP_001317418.1:n.1707-9del