Canonical Allele Identifier: CA222977901

Gene: INCENP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62127972del , CM000673.2:g.62127972del	GRCh38
NC_000011.9:g.61895444del , CM000673.1:g.61895444del	GRCh37
NC_000011.8:g.61652020del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001040694.2:c.-11-179del MANE Select	NP_001035784.1:n.-11-179del
ENST00000394818.8:c.-11-179del MANE Select	ENSP00000378295.3:n.-11-179del
NM_001040694.1:c.-11-179del	NP_001035784.1:n.-11-179del
NM_020238.2:c.-11-179del	NP_064623.2:n.-11-179del
NM_020238.3:c.-11-179del	NP_064623.2:n.-11-179del
ENST00000278849.4:c.-11-179del	ENSP00000278849.4:n.-11-179del
ENST00000394818.7:c.-11-179del	ENSP00000378295.3:n.-11-179del
ENST00000528037.1:n.154-179del
ENST00000533896.5:c.-11-179del	ENSP00000433100.1:n.-11-179del
XM_006718533.1:c.-11-179del	XP_006718596.1:n.-11-179del
XM_006718533.3:c.-11-179del	XP_006718596.1:n.-11-179del
XM_011544995.1:c.-11-179del	XP_011543297.1:n.-11-179del
XM_011544995.3:c.-11-179del	XP_011543297.1:n.-11-179del
XM_011544996.1:c.-11-179del	XP_011543298.1:n.-11-179del
XM_011544996.3:c.-11-179del	XP_011543298.1:n.-11-179del
XM_011544997.1:c.-11-179del	XP_011543299.1:n.-11-179del
XM_011544997.2:c.-11-179del	XP_011543299.1:n.-11-179del
XM_011544998.1:c.-11-179del	XP_011543300.1:n.-11-179del
XM_011544998.3:c.-11-179del	XP_011543300.1:n.-11-179del