Canonical Allele Identifier: CA6041515

Gene: INCENP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62129826G>A , CM000673.2:g.62129826G>A	GRCh38
NC_000011.9:g.61897298G>A , CM000673.1:g.61897298G>A	GRCh37
NC_000011.8:g.61653874G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394818.8:c.299G>A MANE Select	ENSP00000378295.3:p.Arg100His
ENST00000278849.4:c.299G>A	ENSP00000278849.4:p.Arg100His
ENST00000394818.7:c.299G>A	ENSP00000378295.3:p.Arg100His
ENST00000528037.1:n.463G>A
ENST00000533896.5:c.299G>A	ENSP00000433100.1:p.Arg100His
NM_001040694.1:c.299G>A	NP_001035784.1:p.Arg100His
NM_020238.2:c.299G>A	NP_064623.2:p.Arg100His
XM_006718533.1:c.299G>A	XP_006718596.1:p.Arg100His
XM_011544995.1:c.299G>A	XP_011543297.1:p.Arg100His
XM_011544996.1:c.299G>A	XP_011543298.1:p.Arg100His
XM_011544997.1:c.299G>A	XP_011543299.1:p.Arg100His
XM_011544998.1:c.299G>A	XP_011543300.1:p.Arg100His
XM_006718533.3:c.299G>A	XP_006718596.1:p.Arg100His
XM_011544995.3:c.299G>A	XP_011543297.1:p.Arg100His
XM_011544996.3:c.299G>A	XP_011543298.1:p.Arg100His
XM_011544997.2:c.299G>A	XP_011543299.1:p.Arg100His
XM_011544998.3:c.299G>A	XP_011543300.1:p.Arg100His
NM_001040694.2:c.299G>A MANE Select	NP_001035784.1:p.Arg100His
NM_020238.3:c.299G>A	NP_064623.2:p.Arg100His