Canonical Allele Identifier: CA1977633329

Gene: INCENP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62152221C= , CM000673.2:g.62152221C=	GRCh38
NC_000011.9:g.61919693C= , CM000673.1:g.61919693C=	GRCh37
NC_000011.8:g.61676269C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001040694.2:c.*245C= MANE Select	NP_001035784.1:n.*245C=
ENST00000394818.8:c.*245C= MANE Select	ENSP00000378295.3:n.*245C=
NM_001040694.1:c.*245C=	NP_001035784.1:n.*245C=
NM_020238.2:c.*245C=	NP_064623.2:n.*245C=
NM_020238.3:c.*245C=	NP_064623.2:n.*245C=
ENST00000278849.4:c.*245C=	ENSP00000278849.4:n.*245C=
ENST00000394818.7:c.*245C=	ENSP00000378295.3:n.*245C=
XM_006718533.1:c.*245C=	XP_006718596.1:n.*245C=
XM_006718533.3:c.*245C=	XP_006718596.1:n.*245C=
XM_011544995.1:c.*245C=	XP_011543297.1:n.*245C=
XM_011544995.3:c.*245C=	XP_011543297.1:n.*245C=
XM_011544996.1:c.*245C=	XP_011543298.1:n.*245C=
XM_011544996.3:c.*245C=	XP_011543298.1:n.*245C=
XM_011544997.1:c.*245C=	XP_011543299.1:n.*245C=
XM_011544997.2:c.*245C=	XP_011543299.1:n.*245C=
XM_011544998.1:c.*245C=	XP_011543300.1:n.*245C=
XM_011544998.3:c.*245C=	XP_011543300.1:n.*245C=