Canonical Allele Identifier: CA476144182

Gene: HIKESHI

Linked Data

• MyVariant Identifiers: chr11:g.86017502C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.86306460C>T , CM000673.2:g.86306460C>T	GRCh38
NC_000011.9:g.86017502C>T , CM000673.1:g.86017502C>T	GRCh37
NC_000011.8:g.85695150C>T	NCBI36
NG_046865.1:g.9250C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278483.8:c.246C>T MANE Select	ENSP00000278483.3:p.Phe82=
ENST00000278483.7:c.246C>T	ENSP00000278483.3:p.Phe82=
ENST00000528004.5:c.246C>T	ENSP00000433815.1:p.Phe82=
ENST00000530208.1:n.321C>T
ENST00000531485.5:n.236+3982C>T
ENST00000532270.5:n.585C>T
ENST00000533986.5:c.246C>T	ENSP00000432699.1:p.Phe82=
ENST00000618164.1:c.48C>T	ENSP00000482151.1:p.Phe16=
NM_016401.3:c.246C>T	NP_057485.2:p.Phe82=
NR_024596.1:n.321C>T
NR_024597.1:n.268+3982C>T
NR_024598.1:n.268+3982C>T
XM_011545097.1:c.129C>T	XP_011543399.1:p.Phe43=
XR_949963.1:n.469C>T
NM_001322404.1:c.246C>T	NP_001309333.1:p.Phe82=
NM_001322407.1:c.129C>T	NP_001309336.1:p.Phe43=
NM_001322409.1:c.129C>T	NP_001309338.1:p.Phe43=
NR_136324.1:n.468C>T
XM_017017914.2:c.246C>T	XP_016873403.1:p.Phe82=
XM_017017915.1:c.129C>T	XP_016873404.1:p.Phe43=
XR_001747904.2:n.455C>T
XR_949963.3:n.455C>T
NM_016401.4:c.246C>T MANE Select	NP_057485.2:p.Phe82=
NM_001322404.2:c.246C>T	NP_001309333.1:p.Phe82=
NM_001322407.2:c.129C>T	NP_001309336.1:p.Phe43=
NM_001322409.2:c.129C>T	NP_001309338.1:p.Phe43=
NR_024597.2:n.239+3982C>T
NR_024598.2:n.239+3982C>T
NR_136324.2:n.455C>T