Canonical Allele Identifier: CA13384144

Gene: INCENP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62152043C>G , CM000673.2:g.62152043C>G	GRCh38
NC_000011.9:g.61919515C>G , CM000673.1:g.61919515C>G	GRCh37
NC_000011.8:g.61676091C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001040694.2:c.*67C>G MANE Select	NP_001035784.1:n.*67C>G
ENST00000394818.8:c.*67C>G MANE Select	ENSP00000378295.3:n.*67C>G
NM_001040694.1:c.*67C>G	NP_001035784.1:n.*67C>G
NM_020238.2:c.*67C>G	NP_064623.2:n.*67C>G
NM_020238.3:c.*67C>G	NP_064623.2:n.*67C>G
ENST00000278849.4:c.*67C>G	ENSP00000278849.4:n.*67C>G
ENST00000394818.7:c.*67C>G	ENSP00000378295.3:n.*67C>G
XM_006718533.1:c.*67C>G	XP_006718596.1:n.*67C>G
XM_006718533.3:c.*67C>G	XP_006718596.1:n.*67C>G
XM_011544995.1:c.*67C>G	XP_011543297.1:n.*67C>G
XM_011544995.3:c.*67C>G	XP_011543297.1:n.*67C>G
XM_011544996.1:c.*67C>G	XP_011543298.1:n.*67C>G
XM_011544996.3:c.*67C>G	XP_011543298.1:n.*67C>G
XM_011544997.1:c.*67C>G	XP_011543299.1:n.*67C>G
XM_011544997.2:c.*67C>G	XP_011543299.1:n.*67C>G
XM_011544998.1:c.*67C>G	XP_011543300.1:n.*67C>G
XM_011544998.3:c.*67C>G	XP_011543300.1:n.*67C>G