Canonical Allele Identifier: CA6042284

Gene: INCENP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62148851C>A , CM000673.2:g.62148851C>A	GRCh38
NC_000011.9:g.61916323C>A , CM000673.1:g.61916323C>A	GRCh37
NC_000011.8:g.61672899C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001040694.2:c.2391+5C>A MANE Select	NP_001035784.1:n.2391+5C>A
ENST00000394818.8:c.2391+5C>A MANE Select	ENSP00000378295.3:n.2391+5C>A
NM_001040694.1:c.2391+5C>A	NP_001035784.1:n.2391+5C>A
NM_020238.2:c.2379+5C>A	NP_064623.2:n.2379+5C>A
NM_020238.3:c.2379+5C>A	NP_064623.2:n.2379+5C>A
ENST00000278849.4:c.2379+5C>A	ENSP00000278849.4:n.2379+5C>A
ENST00000394818.7:c.2391+5C>A	ENSP00000378295.3:n.2391+5C>A
XM_006718533.1:c.2403+5C>A	XP_006718596.1:n.2403+5C>A
XM_006718533.3:c.2403+5C>A	XP_006718596.1:n.2403+5C>A
XM_011544995.1:c.2408C>A	XP_011543297.1:p.Pro803Gln
XM_011544995.3:c.2408C>A	XP_011543297.1:p.Pro803Gln
XM_011544996.1:c.2396C>A	XP_011543298.1:p.Pro799Gln
XM_011544996.3:c.2396C>A	XP_011543298.1:p.Pro799Gln
XM_011544997.1:c.2396C>A	XP_011543299.1:p.Pro799Gln
XM_011544997.2:c.2396C>A	XP_011543299.1:p.Pro799Gln
XM_011544998.1:c.2384C>A	XP_011543300.1:p.Pro795Gln
XM_011544998.3:c.2384C>A	XP_011543300.1:p.Pro795Gln