Canonical Allele Identifier: CA482430346

Gene: ANAPC5

Linked Data

• gnomAD v4: 12-121318506-C-A
• MyVariant Identifiers: chr12:g.121756309C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121318506C>A , CM000674.2:g.121318506C>A	GRCh38
NC_000012.11:g.121756309C>A , CM000674.1:g.121756309C>A	GRCh37
NC_000012.10:g.120240692C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261819.8:c.1740G>T MANE Select	ENSP00000261819.3:p.Val580=
ENST00000261819.7:c.1740G>T	ENSP00000261819.3:p.Val580=
ENST00000441917.6:c.1404G>T	ENSP00000415061.2:p.Val468=
ENST00000534976.5:n.2396G>T
ENST00000535482.1:c.738G>T	ENSP00000438754.1:p.Val246=
ENST00000535641.5:n.1951G>T
ENST00000539079.5:c.1084G>T
ENST00000541887.5:c.1701G>T	ENSP00000439875.1:p.Val567=
ENST00000544314.5:n.858G>T
ENST00000545218.5:n.983G>T
NM_001137559.1:c.1404G>T	NP_001131031.1:p.Val468=
NM_016237.4:c.1740G>T	NP_057321.2:p.Val580=
XM_005253900.2:c.1701G>T	XP_005253957.1:p.Val567=
XM_006719449.1:c.546G>T	XP_006719512.1:p.Val182=
NM_001330489.1:c.1701G>T	NP_001317418.1:p.Val567=
XM_017019423.2:c.546G>T	XP_016874912.1:p.Val182=
XM_017019424.2:c.546G>T	XP_016874913.1:p.Val182=
NM_016237.5:c.1740G>T MANE Select	NP_057321.2:p.Val580=
NM_001330489.2:c.1701G>T	NP_001317418.1:p.Val567=