Canonical Allele Identifier: CA386960315

Gene: ANAPC5

Linked Data

• MyVariant Identifiers: chr12:g.121756196G>C (hg19) ; chr12:g.121318393G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121318393G>C , CM000674.2:g.121318393G>C	GRCh38
NC_000012.11:g.121756196G>C , CM000674.1:g.121756196G>C	GRCh37
NC_000012.10:g.120240579G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261819.8:c.1777C>G MANE Select	ENSP00000261819.3:p.Arg593Gly
ENST00000261819.7:c.1777C>G	ENSP00000261819.3:p.Arg593Gly
ENST00000441917.6:c.1441C>G	ENSP00000415061.2:p.Arg481Gly
ENST00000534976.5:n.2509C>G
ENST00000535482.1:c.775C>G	ENSP00000438754.1:p.Arg259Gly
ENST00000535641.5:n.1988C>G
ENST00000539079.5:c.1101C>G
ENST00000541887.5:c.1738C>G	ENSP00000439875.1:p.Arg580Gly
ENST00000544314.5:n.895C>G
ENST00000545218.5:n.989-42C>G
NM_001137559.1:c.1441C>G	NP_001131031.1:p.Arg481Gly
NM_016237.4:c.1777C>G	NP_057321.2:p.Arg593Gly
XM_005253900.2:c.1738C>G	XP_005253957.1:p.Arg580Gly
XM_006719449.1:c.583C>G	XP_006719512.1:p.Arg195Gly
NM_001330489.1:c.1738C>G	NP_001317418.1:p.Arg580Gly
XM_017019423.2:c.583C>G	XP_016874912.1:p.Arg195Gly
XM_017019424.2:c.583C>G	XP_016874913.1:p.Arg195Gly
NM_016237.5:c.1777C>G MANE Select	NP_057321.2:p.Arg593Gly
NM_001330489.2:c.1738C>G	NP_001317418.1:p.Arg580Gly