Canonical Allele Identifier: CA382016148

Gene: HIKESHI

Linked Data

• MyVariant Identifiers: chr11:g.86017296G>T (hg19) ; chr11:g.86306254G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.86306254G>T , CM000673.2:g.86306254G>T	GRCh38
NC_000011.9:g.86017296G>T , CM000673.1:g.86017296G>T	GRCh37
NC_000011.8:g.85694944G>T	NCBI36
NG_046865.1:g.9044G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000278483.8:c.40G>T MANE Select	ENSP00000278483.3:p.Ala14Ser
ENST00000278483.7:c.40G>T	ENSP00000278483.3:p.Ala14Ser
ENST00000528004.5:c.40G>T	ENSP00000433815.1:p.Ala14Ser
ENST00000530208.1:n.115G>T
ENST00000531485.5:n.236+3776G>T
ENST00000532270.5:n.379G>T
ENST00000533986.5:c.40G>T	ENSP00000432699.1:p.Ala14Ser
NM_016401.3:c.40G>T	NP_057485.2:p.Ala14Ser
NR_024596.1:n.115G>T
NR_024597.1:n.268+3776G>T
NR_024598.1:n.268+3776G>T
XM_011545097.1:c.-78G>T	XP_011543399.1:n.-78G>T
XR_949963.1:n.263G>T
NM_001322404.1:c.40G>T	NP_001309333.1:p.Ala14Ser
NM_001322407.1:c.-78G>T	NP_001309336.1:n.-78G>T
NM_001322409.1:c.-78G>T	NP_001309338.1:n.-78G>T
NR_136324.1:n.262G>T
XM_017017914.2:c.40G>T	XP_016873403.1:p.Ala14Ser
XM_017017915.1:c.-78G>T	XP_016873404.1:n.-78G>T
XR_001747904.2:n.249G>T
XR_949963.3:n.249G>T
NM_016401.4:c.40G>T MANE Select	NP_057485.2:p.Ala14Ser
NM_001322404.2:c.40G>T	NP_001309333.1:p.Ala14Ser
NM_001322407.2:c.-78G>T	NP_001309336.1:n.-78G>T
NM_001322409.2:c.-78G>T	NP_001309338.1:n.-78G>T
NR_024597.2:n.239+3776G>T
NR_024598.2:n.239+3776G>T
NR_136324.2:n.249G>T