Canonical Allele Identifier: CA1988521207
Gene: HIKESHI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86306563C= , CM000673.2:g.86306563C= GRCh38
NC_000011.9:g.86017605C= , CM000673.1:g.86017605C= GRCh37
NC_000011.8:g.85695253C= NCBI36
NG_046865.1:g.9353C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278483.8:c.268+81C= MANE Select ENSP00000278483.3:n.268+81C=
ENST00000278483.7:c.268+81C= ENSP00000278483.3:n.268+81C=
ENST00000528004.5:c.268+81C= ENSP00000433815.1:n.268+81C=
ENST00000530208.1:n.343+81C=
ENST00000531485.5:n.236+4085C=
ENST00000532270.5:n.607+81C=
ENST00000533986.5:c.268+81C= ENSP00000432699.1:n.268+81C=
ENST00000618164.1:c.70+81C= ENSP00000482151.1:n.70+81C=
NM_016401.3:c.268+81C= NP_057485.2:n.268+81C=
NR_024596.1:n.343+81C=
NR_024597.1:n.268+4085C=
NR_024598.1:n.268+4085C=
XM_011545097.1:c.151+81C= XP_011543399.1:n.151+81C=
XR_949963.1:n.491+81C=
NM_001322404.1:c.268+81C= NP_001309333.1:n.268+81C=
NM_001322407.1:c.151+81C= NP_001309336.1:n.151+81C=
NM_001322409.1:c.151+81C= NP_001309338.1:n.151+81C=
NR_136324.1:n.490+81C=
XM_017017914.2:c.268+81C= XP_016873403.1:n.268+81C=
XM_017017915.1:c.151+81C= XP_016873404.1:n.151+81C=
XR_001747904.2:n.477+81C=
XR_949963.3:n.477+81C=
NM_016401.4:c.268+81C= MANE Select NP_057485.2:n.268+81C=
NM_001322404.2:c.268+81C= NP_001309333.1:n.268+81C=
NM_001322407.2:c.151+81C= NP_001309336.1:n.151+81C=
NM_001322409.2:c.151+81C= NP_001309338.1:n.151+81C=
NR_024597.2:n.239+4085C=
NR_024598.2:n.239+4085C=
NR_136324.2:n.477+81C=