Canonical Allele Identifier: CA476144139

Gene: HIKESHI

Linked Data

• MyVariant Identifiers: chr11:g.86017433T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.86306391T>C , CM000673.2:g.86306391T>C	GRCh38
NC_000011.9:g.86017433T>C , CM000673.1:g.86017433T>C	GRCh37
NC_000011.8:g.85695081T>C	NCBI36
NG_046865.1:g.9181T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278483.8:c.177T>C MANE Select	ENSP00000278483.3:p.Pro59=
ENST00000278483.7:c.177T>C	ENSP00000278483.3:p.Pro59=
ENST00000528004.5:c.177T>C	ENSP00000433815.1:p.Pro59=
ENST00000530208.1:n.252T>C
ENST00000531485.5:n.236+3913T>C
ENST00000532270.5:n.516T>C
ENST00000533986.5:c.177T>C	ENSP00000432699.1:p.Pro59=
ENST00000618164.1:c.-21T>C	ENSP00000482151.1:n.-21T>C
NM_016401.3:c.177T>C	NP_057485.2:p.Pro59=
NR_024596.1:n.252T>C
NR_024597.1:n.268+3913T>C
NR_024598.1:n.268+3913T>C
XM_011545097.1:c.60T>C	XP_011543399.1:p.Pro20=
XR_949963.1:n.400T>C
NM_001322404.1:c.177T>C	NP_001309333.1:p.Pro59=
NM_001322407.1:c.60T>C	NP_001309336.1:p.Pro20=
NM_001322409.1:c.60T>C	NP_001309338.1:p.Pro20=
NR_136324.1:n.399T>C
XM_017017914.2:c.177T>C	XP_016873403.1:p.Pro59=
XM_017017915.1:c.60T>C	XP_016873404.1:p.Pro20=
XR_001747904.2:n.386T>C
XR_949963.3:n.386T>C
NM_016401.4:c.177T>C MANE Select	NP_057485.2:p.Pro59=
NM_001322404.2:c.177T>C	NP_001309333.1:p.Pro59=
NM_001322407.2:c.60T>C	NP_001309336.1:p.Pro20=
NM_001322409.2:c.60T>C	NP_001309338.1:p.Pro20=
NR_024597.2:n.239+3913T>C
NR_024598.2:n.239+3913T>C
NR_136324.2:n.386T>C