Canonical Allele Identifier: CA608060696

Gene: ANAPC5

Linked Data

• dbSNP Id: rs771701266
• gnomAD v2: 12-121756289-C-T
• gnomAD v4: 12-121318486-C-T
• MyVariant Identifiers: chr12:g.121756289C>T (hg19) ; chr12:g.121318486C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121318486C>T , CM000674.2:g.121318486C>T	GRCh38
NC_000012.11:g.121756289C>T , CM000674.1:g.121756289C>T	GRCh37
NC_000012.10:g.120240672C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261819.8:c.1745+15G>A MANE Select	ENSP00000261819.3:n.1745+15G>A
ENST00000261819.7:c.1745+15G>A	ENSP00000261819.3:n.1745+15G>A
ENST00000441917.6:c.1409+15G>A	ENSP00000415061.2:n.1409+15G>A
ENST00000534976.5:n.2416G>A
ENST00000535482.1:c.743+15G>A	ENSP00000438754.1:n.743+15G>A
ENST00000535641.5:n.1956+15G>A
ENST00000539079.5:c.1089+15G>A
ENST00000541887.5:c.1706+15G>A	ENSP00000439875.1:n.1706+15G>A
ENST00000544314.5:n.863+15G>A
ENST00000545218.5:n.988+15G>A
NM_001137559.1:c.1409+15G>A	NP_001131031.1:n.1409+15G>A
NM_016237.4:c.1745+15G>A	NP_057321.2:n.1745+15G>A
XM_005253900.2:c.1706+15G>A	XP_005253957.1:n.1706+15G>A
XM_006719449.1:c.551+15G>A	XP_006719512.1:n.551+15G>A
NM_001330489.1:c.1706+15G>A	NP_001317418.1:n.1706+15G>A
XM_017019423.2:c.551+15G>A	XP_016874912.1:n.551+15G>A
XM_017019424.2:c.551+15G>A	XP_016874913.1:n.551+15G>A
NM_016237.5:c.1745+15G>A MANE Select	NP_057321.2:n.1745+15G>A
NM_001330489.2:c.1706+15G>A	NP_001317418.1:n.1706+15G>A