Canonical Allele Identifier: CA482430364

Gene: ANAPC5

Linked Data

• MyVariant Identifiers: chr12:g.121756342A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121318539A>T , CM000674.2:g.121318539A>T	GRCh38
NC_000012.11:g.121756342A>T , CM000674.1:g.121756342A>T	GRCh37
NC_000012.10:g.120240725A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261819.8:c.1707T>A MANE Select	ENSP00000261819.3:p.Val569=
ENST00000261819.7:c.1707T>A	ENSP00000261819.3:p.Val569=
ENST00000366333.3:n.919T>A
ENST00000441917.6:c.1371T>A	ENSP00000415061.2:p.Val457=
ENST00000534976.5:n.2363T>A
ENST00000535482.1:c.705T>A	ENSP00000438754.1:p.Val235=
ENST00000535641.5:n.1918T>A
ENST00000539079.5:c.1051T>A
ENST00000541887.5:c.1668T>A	ENSP00000439875.1:p.Val556=
ENST00000544314.5:n.825T>A
ENST00000545218.5:n.950T>A
NM_001137559.1:c.1371T>A	NP_001131031.1:p.Val457=
NM_016237.4:c.1707T>A	NP_057321.2:p.Val569=
XM_005253900.2:c.1668T>A	XP_005253957.1:p.Val556=
XM_006719449.1:c.513T>A	XP_006719512.1:p.Val171=
NM_001330489.1:c.1668T>A	NP_001317418.1:p.Val556=
XM_017019423.2:c.513T>A	XP_016874912.1:p.Val171=
XM_017019424.2:c.513T>A	XP_016874913.1:p.Val171=
NM_016237.5:c.1707T>A MANE Select	NP_057321.2:p.Val569=
NM_001330489.2:c.1668T>A	NP_001317418.1:p.Val556=