Canonical Allele Identifier: CA6835168

Gene: ANAPC5

Linked Data

• dbSNP Id: rs749092418
• ExAC: 12:121756200 G / A
• gnomAD v2: 12-121756200-G-A
• gnomAD v3: 12-121318397-G-A
• gnomAD v4: 12-121318397-G-A
• MyVariant Identifiers: chr12:g.121756200G>A (hg19) ; chr12:g.121318397G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121318397G>A , CM000674.2:g.121318397G>A	GRCh38
NC_000012.11:g.121756200G>A , CM000674.1:g.121756200G>A	GRCh37
NC_000012.10:g.120240583G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261819.8:c.1773C>T MANE Select	ENSP00000261819.3:p.Tyr591=
ENST00000261819.7:c.1773C>T	ENSP00000261819.3:p.Tyr591=
ENST00000441917.6:c.1437C>T	ENSP00000415061.2:p.Tyr479=
ENST00000534976.5:n.2505C>T
ENST00000535482.1:c.771C>T	ENSP00000438754.1:p.Tyr257=
ENST00000535641.5:n.1984C>T
ENST00000539079.5:c.1097C>T
ENST00000541887.5:c.1734C>T	ENSP00000439875.1:p.Tyr578=
ENST00000544314.5:n.891C>T
ENST00000545218.5:n.989-46C>T
NM_001137559.1:c.1437C>T	NP_001131031.1:p.Tyr479=
NM_016237.4:c.1773C>T	NP_057321.2:p.Tyr591=
XM_005253900.2:c.1734C>T	XP_005253957.1:p.Tyr578=
XM_006719449.1:c.579C>T	XP_006719512.1:p.Tyr193=
NM_001330489.1:c.1734C>T	NP_001317418.1:p.Tyr578=
XM_017019423.2:c.579C>T	XP_016874912.1:p.Tyr193=
XM_017019424.2:c.579C>T	XP_016874913.1:p.Tyr193=
NM_016237.5:c.1773C>T MANE Select	NP_057321.2:p.Tyr591=
NM_001330489.2:c.1734C>T	NP_001317418.1:p.Tyr578=