Canonical Allele Identifier: CA222975436

Gene: INCENP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62150370T>C , CM000673.2:g.62150370T>C	GRCh38
NC_000011.9:g.61917842T>C , CM000673.1:g.61917842T>C	GRCh37
NC_000011.8:g.61674418T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001040694.2:c.2542+163T>C MANE Select	NP_001035784.1:n.2542+163T>C
ENST00000394818.8:c.2542+163T>C MANE Select	ENSP00000378295.3:n.2542+163T>C
NM_001040694.1:c.2542+163T>C	NP_001035784.1:n.2542+163T>C
NM_020238.2:c.2530+163T>C	NP_064623.2:n.2530+163T>C
NM_020238.3:c.2530+163T>C	NP_064623.2:n.2530+163T>C
ENST00000278849.4:c.2530+163T>C	ENSP00000278849.4:n.2530+163T>C
ENST00000394818.7:c.2542+163T>C	ENSP00000378295.3:n.2542+163T>C
XM_006718533.1:c.2554+163T>C	XP_006718596.1:n.2554+163T>C
XM_006718533.3:c.2554+163T>C	XP_006718596.1:n.2554+163T>C
XM_011544995.1:c.2587+163T>C	XP_011543297.1:n.2587+163T>C
XM_011544995.3:c.2587+163T>C	XP_011543297.1:n.2587+163T>C
XM_011544996.1:c.2575+163T>C	XP_011543298.1:n.2575+163T>C
XM_011544996.3:c.2575+163T>C	XP_011543298.1:n.2575+163T>C
XM_011544997.1:c.2575+163T>C	XP_011543299.1:n.2575+163T>C
XM_011544997.2:c.2575+163T>C	XP_011543299.1:n.2575+163T>C
XM_011544998.1:c.2563+163T>C	XP_011543300.1:n.2563+163T>C
XM_011544998.3:c.2563+163T>C	XP_011543300.1:n.2563+163T>C