Canonical Allele Identifier: CA6042378

Gene: INCENP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62151919G>A , CM000673.2:g.62151919G>A	GRCh38
NC_000011.9:g.61919391G>A , CM000673.1:g.61919391G>A	GRCh37
NC_000011.8:g.61675967G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394818.8:c.2700G>A MANE Select	ENSP00000378295.3:p.Pro900=
ENST00000278849.4:c.2688G>A	ENSP00000278849.4:p.Pro896=
ENST00000394818.7:c.2700G>A	ENSP00000378295.3:p.Pro900=
NM_001040694.1:c.2700G>A	NP_001035784.1:p.Pro900=
NM_020238.2:c.2688G>A	NP_064623.2:p.Pro896=
XM_006718533.1:c.2712G>A	XP_006718596.1:p.Pro904=
XM_011544995.1:c.2745G>A	XP_011543297.1:p.Pro915=
XM_011544996.1:c.2733G>A	XP_011543298.1:p.Pro911=
XM_011544997.1:c.2733G>A	XP_011543299.1:p.Pro911=
XM_011544998.1:c.2721G>A	XP_011543300.1:p.Pro907=
XM_006718533.3:c.2712G>A	XP_006718596.1:p.Pro904=
XM_011544995.3:c.2745G>A	XP_011543297.1:p.Pro915=
XM_011544996.3:c.2733G>A	XP_011543298.1:p.Pro911=
XM_011544997.2:c.2733G>A	XP_011543299.1:p.Pro911=
XM_011544998.3:c.2721G>A	XP_011543300.1:p.Pro907=
NM_001040694.2:c.2700G>A MANE Select	NP_001035784.1:p.Pro900=
NM_020238.3:c.2688G>A	NP_064623.2:p.Pro896=