Canonical Allele Identifier: CA13519997

Gene: INCENP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62140437A>G , CM000673.2:g.62140437A>G	GRCh38
NC_000011.9:g.61907909A>G , CM000673.1:g.61907909A>G	GRCh37
NC_000011.8:g.61664485A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001040694.2:c.1343+152A>G MANE Select	NP_001035784.1:n.1343+152A>G
ENST00000394818.8:c.1343+152A>G MANE Select	ENSP00000378295.3:n.1343+152A>G
NM_001040694.1:c.1343+152A>G	NP_001035784.1:n.1343+152A>G
NM_020238.2:c.1343+152A>G	NP_064623.2:n.1343+152A>G
NM_020238.3:c.1343+152A>G	NP_064623.2:n.1343+152A>G
ENST00000278849.4:c.1343+152A>G	ENSP00000278849.4:n.1343+152A>G
ENST00000394818.7:c.1343+152A>G	ENSP00000378295.3:n.1343+152A>G
ENST00000528375.1:n.312+152A>G
XM_006718533.1:c.1343+152A>G	XP_006718596.1:n.1343+152A>G
XM_006718533.3:c.1343+152A>G	XP_006718596.1:n.1343+152A>G
XM_011544995.1:c.1343+152A>G	XP_011543297.1:n.1343+152A>G
XM_011544995.3:c.1343+152A>G	XP_011543297.1:n.1343+152A>G
XM_011544996.1:c.1343+152A>G	XP_011543298.1:n.1343+152A>G
XM_011544996.3:c.1343+152A>G	XP_011543298.1:n.1343+152A>G
XM_011544997.1:c.1343+152A>G	XP_011543299.1:n.1343+152A>G
XM_011544997.2:c.1343+152A>G	XP_011543299.1:n.1343+152A>G
XM_011544998.1:c.1343+152A>G	XP_011543300.1:n.1343+152A>G
XM_011544998.3:c.1343+152A>G	XP_011543300.1:n.1343+152A>G