Canonical Allele Identifier: CA386961263

Gene: ANAPC5

Linked Data

• MyVariant Identifiers: chr12:g.121756376G>T (hg19) ; chr12:g.121318573G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121318573G>T , CM000674.2:g.121318573G>T	GRCh38
NC_000012.11:g.121756376G>T , CM000674.1:g.121756376G>T	GRCh37
NC_000012.10:g.120240759G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261819.8:c.1673C>A MANE Select	ENSP00000261819.3:p.Ser558Ter
ENST00000261819.7:c.1673C>A	ENSP00000261819.3:p.Ser558Ter
ENST00000366333.3:n.885C>A
ENST00000441917.6:c.1337C>A	ENSP00000415061.2:p.Ser446Ter
ENST00000534976.5:n.2329C>A
ENST00000535482.1:c.671C>A	ENSP00000438754.1:p.Ser224Ter
ENST00000535641.5:n.1884C>A
ENST00000539079.5:c.1017C>A
ENST00000541887.5:c.1634C>A	ENSP00000439875.1:p.Ser545Ter
ENST00000544314.5:n.791C>A
ENST00000545218.5:n.916C>A
NM_001137559.1:c.1337C>A	NP_001131031.1:p.Ser446Ter
NM_016237.4:c.1673C>A	NP_057321.2:p.Ser558Ter
XM_005253900.2:c.1634C>A	XP_005253957.1:p.Ser545Ter
XM_006719449.1:c.479C>A	XP_006719512.1:p.Ser160Ter
NM_001330489.1:c.1634C>A	NP_001317418.1:p.Ser545Ter
XM_017019423.2:c.479C>A	XP_016874912.1:p.Ser160Ter
XM_017019424.2:c.479C>A	XP_016874913.1:p.Ser160Ter
NM_016237.5:c.1673C>A MANE Select	NP_057321.2:p.Ser558Ter
NM_001330489.2:c.1634C>A	NP_001317418.1:p.Ser545Ter