Canonical Allele Identifier: CA2575323931

Gene: ANAPC5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121318436G>C , CM000674.2:g.121318436G>C	GRCh38
NC_000012.11:g.121756239G>C , CM000674.1:g.121756239G>C	GRCh37
NC_000012.10:g.120240622G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261819.8:c.1746-12C>G MANE Select	ENSP00000261819.3:n.1746-12C>G
ENST00000261819.7:c.1746-12C>G	ENSP00000261819.3:n.1746-12C>G
ENST00000441917.6:c.1410-12C>G	ENSP00000415061.2:n.1410-12C>G
ENST00000534976.5:n.2466C>G
ENST00000535482.1:c.744-12C>G	ENSP00000438754.1:n.744-12C>G
ENST00000535641.5:n.1957-12C>G
ENST00000539079.5:c.1090-32C>G
ENST00000541887.5:c.1707-12C>G	ENSP00000439875.1:n.1707-12C>G
ENST00000544314.5:n.864-12C>G
ENST00000545218.5:n.988+65C>G
NM_001137559.1:c.1410-12C>G	NP_001131031.1:n.1410-12C>G
NM_016237.4:c.1746-12C>G	NP_057321.2:n.1746-12C>G
XM_005253900.2:c.1707-12C>G	XP_005253957.1:n.1707-12C>G
XM_006719449.1:c.552-12C>G	XP_006719512.1:n.552-12C>G
NM_001330489.1:c.1707-12C>G	NP_001317418.1:n.1707-12C>G
XM_017019423.2:c.552-12C>G	XP_016874912.1:n.552-12C>G
XM_017019424.2:c.552-12C>G	XP_016874913.1:n.552-12C>G
NM_016237.5:c.1746-12C>G MANE Select	NP_057321.2:n.1746-12C>G
NM_001330489.2:c.1707-12C>G	NP_001317418.1:n.1707-12C>G