Canonical Allele Identifier: CA1988521137

Gene: HIKESHI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.86306392G= , CM000673.2:g.86306392G=	GRCh38
NC_000011.9:g.86017434G= , CM000673.1:g.86017434G=	GRCh37
NC_000011.8:g.85695082G=	NCBI36
NG_046865.1:g.9182G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278483.8:c.178G= MANE Select	ENSP00000278483.3:p.Asp60=
ENST00000278483.7:c.178G=	ENSP00000278483.3:p.Asp60=
ENST00000528004.5:c.178G=	ENSP00000433815.1:p.Asp60=
ENST00000530208.1:n.253G=
ENST00000531485.5:n.236+3914G=
ENST00000532270.5:n.517G=
ENST00000533986.5:c.178G=	ENSP00000432699.1:p.Asp60=
ENST00000618164.1:c.-20G=	ENSP00000482151.1:n.-20G=
NM_016401.3:c.178G=	NP_057485.2:p.Asp60=
NR_024596.1:n.253G=
NR_024597.1:n.268+3914G=
NR_024598.1:n.268+3914G=
XM_011545097.1:c.61G=	XP_011543399.1:p.Asp21=
XR_949963.1:n.401G=
NM_001322404.1:c.178G=	NP_001309333.1:p.Asp60=
NM_001322407.1:c.61G=	NP_001309336.1:p.Asp21=
NM_001322409.1:c.61G=	NP_001309338.1:p.Asp21=
NR_136324.1:n.400G=
XM_017017914.2:c.178G=	XP_016873403.1:p.Asp60=
XM_017017915.1:c.61G=	XP_016873404.1:p.Asp21=
XR_001747904.2:n.387G=
XR_949963.3:n.387G=
NM_016401.4:c.178G= MANE Select	NP_057485.2:p.Asp60=
NM_001322404.2:c.178G=	NP_001309333.1:p.Asp60=
NM_001322407.2:c.61G=	NP_001309336.1:p.Asp21=
NM_001322409.2:c.61G=	NP_001309338.1:p.Asp21=
NR_024597.2:n.239+3914G=
NR_024598.2:n.239+3914G=
NR_136324.2:n.387G=