Canonical Allele Identifier: CA382016528
Gene: HIKESHI HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86306287T>C , CM000673.2:g.86306287T>C GRCh38
NC_000011.9:g.86017329T>C , CM000673.1:g.86017329T>C GRCh37
NC_000011.8:g.85694977T>C NCBI36
NG_046865.1:g.9077T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000278483.8:c.73T>C MANE Select ENSP00000278483.3:p.Phe25Leu
ENST00000278483.7:c.73T>C ENSP00000278483.3:p.Phe25Leu
ENST00000528004.5:c.73T>C ENSP00000433815.1:p.Phe25Leu
ENST00000530208.1:n.148T>C
ENST00000531485.5:n.236+3809T>C
ENST00000532270.5:n.412T>C
ENST00000533986.5:c.73T>C ENSP00000432699.1:p.Phe25Leu
NM_016401.3:c.73T>C NP_057485.2:p.Phe25Leu
NR_024596.1:n.148T>C
NR_024597.1:n.268+3809T>C
NR_024598.1:n.268+3809T>C
XM_011545097.1:c.-45T>C XP_011543399.1:n.-45T>C
XR_949963.1:n.296T>C
NM_001322404.1:c.73T>C NP_001309333.1:p.Phe25Leu
NM_001322407.1:c.-45T>C NP_001309336.1:n.-45T>C
NM_001322409.1:c.-45T>C NP_001309338.1:n.-45T>C
NR_136324.1:n.295T>C
XM_017017914.2:c.73T>C XP_016873403.1:p.Phe25Leu
XM_017017915.1:c.-45T>C XP_016873404.1:n.-45T>C
XR_001747904.2:n.282T>C
XR_949963.3:n.282T>C
NM_016401.4:c.73T>C MANE Select NP_057485.2:p.Phe25Leu
NM_001322404.2:c.73T>C NP_001309333.1:p.Phe25Leu
NM_001322407.2:c.-45T>C NP_001309336.1:n.-45T>C
NM_001322409.2:c.-45T>C NP_001309338.1:n.-45T>C
NR_024597.2:n.239+3809T>C
NR_024598.2:n.239+3809T>C
NR_136324.2:n.282T>C