Canonical Allele Identifier: CA482430358

Gene: ANAPC5

Linked Data

• MyVariant Identifiers: chr12:g.121756330T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121318527T>C , CM000674.2:g.121318527T>C	GRCh38
NC_000012.11:g.121756330T>C , CM000674.1:g.121756330T>C	GRCh37
NC_000012.10:g.120240713T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261819.8:c.1719A>G MANE Select	ENSP00000261819.3:p.Lys573=
ENST00000261819.7:c.1719A>G	ENSP00000261819.3:p.Lys573=
ENST00000441917.6:c.1383A>G	ENSP00000415061.2:p.Lys461=
ENST00000534976.5:n.2375A>G
ENST00000535482.1:c.717A>G	ENSP00000438754.1:p.Lys239=
ENST00000535641.5:n.1930A>G
ENST00000539079.5:c.1063A>G
ENST00000541887.5:c.1680A>G	ENSP00000439875.1:p.Lys560=
ENST00000544314.5:n.837A>G
ENST00000545218.5:n.962A>G
NM_001137559.1:c.1383A>G	NP_001131031.1:p.Lys461=
NM_016237.4:c.1719A>G	NP_057321.2:p.Lys573=
XM_005253900.2:c.1680A>G	XP_005253957.1:p.Lys560=
XM_006719449.1:c.525A>G	XP_006719512.1:p.Lys175=
NM_001330489.1:c.1680A>G	NP_001317418.1:p.Lys560=
XM_017019423.2:c.525A>G	XP_016874912.1:p.Lys175=
XM_017019424.2:c.525A>G	XP_016874913.1:p.Lys175=
NM_016237.5:c.1719A>G MANE Select	NP_057321.2:p.Lys573=
NM_001330489.2:c.1680A>G	NP_001317418.1:p.Lys560=