Canonical Allele Identifier: CA6042308

Gene: INCENP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62150080G>C , CM000673.2:g.62150080G>C	GRCh38
NC_000011.9:g.61917552G>C , CM000673.1:g.61917552G>C	GRCh37
NC_000011.8:g.61674128G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001040694.2:c.2415G>C MANE Select	NP_001035784.1:p.Gln805His
ENST00000394818.8:c.2415G>C MANE Select	ENSP00000378295.3:p.Gln805His
NM_001040694.1:c.2415G>C	NP_001035784.1:p.Gln805His
NM_020238.2:c.2403G>C	NP_064623.2:p.Gln801His
NM_020238.3:c.2403G>C	NP_064623.2:p.Gln801His
ENST00000278849.4:c.2403G>C	ENSP00000278849.4:p.Gln801His
ENST00000394818.7:c.2415G>C	ENSP00000378295.3:p.Gln805His
XM_006718533.1:c.2427G>C	XP_006718596.1:p.Gln809His
XM_006718533.3:c.2427G>C	XP_006718596.1:p.Gln809His
XM_011544995.1:c.2460G>C	XP_011543297.1:p.Gln820His
XM_011544995.3:c.2460G>C	XP_011543297.1:p.Gln820His
XM_011544996.1:c.2448G>C	XP_011543298.1:p.Gln816His
XM_011544996.3:c.2448G>C	XP_011543298.1:p.Gln816His
XM_011544997.1:c.2448G>C	XP_011543299.1:p.Gln816His
XM_011544997.2:c.2448G>C	XP_011543299.1:p.Gln816His
XM_011544998.1:c.2436G>C	XP_011543300.1:p.Gln812His
XM_011544998.3:c.2436G>C	XP_011543300.1:p.Gln812His