Canonical Allele Identifier: CA1988521142

Gene: HIKESHI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.86306407C= , CM000673.2:g.86306407C=	GRCh38
NC_000011.9:g.86017449C= , CM000673.1:g.86017449C=	GRCh37
NC_000011.8:g.85695097C=	NCBI36
NG_046865.1:g.9197C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278483.8:c.193C= MANE Select	ENSP00000278483.3:p.Pro65=
ENST00000278483.7:c.193C=	ENSP00000278483.3:p.Pro65=
ENST00000528004.5:c.193C=	ENSP00000433815.1:p.Pro65=
ENST00000530208.1:n.268C=
ENST00000531485.5:n.236+3929C=
ENST00000532270.5:n.532C=
ENST00000533986.5:c.193C=	ENSP00000432699.1:p.Pro65=
ENST00000618164.1:c.-5C=	ENSP00000482151.1:n.-5C=
NM_016401.3:c.193C=	NP_057485.2:p.Pro65=
NR_024596.1:n.268C=
NR_024597.1:n.268+3929C=
NR_024598.1:n.268+3929C=
XM_011545097.1:c.76C=	XP_011543399.1:p.Pro26=
XR_949963.1:n.416C=
NM_001322404.1:c.193C=	NP_001309333.1:p.Pro65=
NM_001322407.1:c.76C=	NP_001309336.1:p.Pro26=
NM_001322409.1:c.76C=	NP_001309338.1:p.Pro26=
NR_136324.1:n.415C=
XM_017017914.2:c.193C=	XP_016873403.1:p.Pro65=
XM_017017915.1:c.76C=	XP_016873404.1:p.Pro26=
XR_001747904.2:n.402C=
XR_949963.3:n.402C=
NM_016401.4:c.193C= MANE Select	NP_057485.2:p.Pro65=
NM_001322404.2:c.193C=	NP_001309333.1:p.Pro65=
NM_001322407.2:c.76C=	NP_001309336.1:p.Pro26=
NM_001322409.2:c.76C=	NP_001309338.1:p.Pro26=
NR_024597.2:n.239+3929C=
NR_024598.2:n.239+3929C=
NR_136324.2:n.402C=