Canonical Allele Identifier: CA348222599

Gene: ANAPC1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111794817C>T , CM000664.2:g.111794817C>T	GRCh38
NC_000002.11:g.112552394C>T , CM000664.1:g.112552394C>T	GRCh37
NC_000002.10:g.112268865C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341068.8:c.4373+1G>A MANE Select	ENSP00000339109.3:n.4373+1G>A
ENST00000341068.7:c.4373+1G>A	ENSP00000339109.3:n.4373+1G>A
ENST00000427997.5:c.2976+1G>A
ENST00000464695.1:n.223+1G>A
NM_022662.3:c.4373+1G>A	NP_073153.1:n.4373+1G>A
XM_011511633.1:c.4385+1G>A	XP_011509935.1:n.4385+1G>A
XM_011511634.1:c.4091+1G>A	XP_011509936.1:n.4091+1G>A
XM_011511635.1:c.3905+1G>A	XP_011509937.1:n.3905+1G>A
XM_011511633.2:c.4385+1G>A	XP_011509935.1:n.4385+1G>A
XM_011511634.2:c.4091+1G>A	XP_011509936.1:n.4091+1G>A
XM_017004710.2:c.4385+1G>A	XP_016860199.1:n.4385+1G>A
XM_017004711.1:c.4373+1G>A	XP_016860200.1:n.4373+1G>A
XM_017004712.2:c.4079+1G>A	XP_016860201.1:n.4079+1G>A
XM_017004713.1:c.3905+1G>A	XP_016860202.1:n.3905+1G>A
XM_017004714.1:c.3893+1G>A	XP_016860203.1:n.3893+1G>A
NM_022662.4:c.4373+1G>A MANE Select	NP_073153.1:n.4373+1G>A