Canonical Allele Identifier: CA1988521162
Gene: HIKESHI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86306451T= , CM000673.2:g.86306451T= GRCh38
NC_000011.9:g.86017493T= , CM000673.1:g.86017493T= GRCh37
NC_000011.8:g.85695141T= NCBI36
NG_046865.1:g.9241T=

Transcript Alleles

HGVS Amino-acid change
ENST00000278483.8:c.237T= MANE Select ENSP00000278483.3:p.Ser79=
ENST00000278483.7:c.237T= ENSP00000278483.3:p.Ser79=
ENST00000528004.5:c.237T= ENSP00000433815.1:p.Ser79=
ENST00000530208.1:n.312T=
ENST00000531485.5:n.236+3973T=
ENST00000532270.5:n.576T=
ENST00000533986.5:c.237T= ENSP00000432699.1:p.Ser79=
ENST00000618164.1:c.39T= ENSP00000482151.1:p.Ser13=
NM_016401.3:c.237T= NP_057485.2:p.Ser79=
NR_024596.1:n.312T=
NR_024597.1:n.268+3973T=
NR_024598.1:n.268+3973T=
XM_011545097.1:c.120T= XP_011543399.1:p.Ser40=
XR_949963.1:n.460T=
NM_001322404.1:c.237T= NP_001309333.1:p.Ser79=
NM_001322407.1:c.120T= NP_001309336.1:p.Ser40=
NM_001322409.1:c.120T= NP_001309338.1:p.Ser40=
NR_136324.1:n.459T=
XM_017017914.2:c.237T= XP_016873403.1:p.Ser79=
XM_017017915.1:c.120T= XP_016873404.1:p.Ser40=
XR_001747904.2:n.446T=
XR_949963.3:n.446T=
NM_016401.4:c.237T= MANE Select NP_057485.2:p.Ser79=
NM_001322404.2:c.237T= NP_001309333.1:p.Ser79=
NM_001322407.2:c.120T= NP_001309336.1:p.Ser40=
NM_001322409.2:c.120T= NP_001309338.1:p.Ser40=
NR_024597.2:n.239+3973T=
NR_024598.2:n.239+3973T=
NR_136324.2:n.446T=