Canonical Allele Identifier: CA2615436848

Gene: HIKESHI

Linked Data

• gnomAD v4: 11-86306559-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.86306559_86306560insC , CM000673.2:g.86306559_86306560insC	GRCh38
NC_000011.9:g.86017601_86017602insC , CM000673.1:g.86017601_86017602insC	GRCh37
NC_000011.8:g.85695249_85695250insC	NCBI36
NG_046865.1:g.9349_9350insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278483.8:c.268+77_268+78insC MANE Select	ENSP00000278483.3:n.268+77_268+78insC
ENST00000278483.7:c.268+77_268+78insC	ENSP00000278483.3:n.268+77_268+78insC
ENST00000528004.5:c.268+77_268+78insC	ENSP00000433815.1:n.268+77_268+78insC
ENST00000530208.1:n.343+77_343+78insC
ENST00000531485.5:n.236+4081_236+4082insC
ENST00000532270.5:n.607+77_607+78insC
ENST00000533986.5:c.268+77_268+78insC	ENSP00000432699.1:n.268+77_268+78insC
ENST00000618164.1:c.70+77_70+78insC	ENSP00000482151.1:n.70+77_70+78insC
NM_016401.3:c.268+77_268+78insC	NP_057485.2:n.268+77_268+78insC
NR_024596.1:n.343+77_343+78insC
NR_024597.1:n.268+4081_268+4082insC
NR_024598.1:n.268+4081_268+4082insC
XM_011545097.1:c.151+77_151+78insC	XP_011543399.1:n.151+77_151+78insC
XR_949963.1:n.491+77_491+78insC
NM_001322404.1:c.268+77_268+78insC	NP_001309333.1:n.268+77_268+78insC
NM_001322407.1:c.151+77_151+78insC	NP_001309336.1:n.151+77_151+78insC
NM_001322409.1:c.151+77_151+78insC	NP_001309338.1:n.151+77_151+78insC
NR_136324.1:n.490+77_490+78insC
XM_017017914.2:c.268+77_268+78insC	XP_016873403.1:n.268+77_268+78insC
XM_017017915.1:c.151+77_151+78insC	XP_016873404.1:n.151+77_151+78insC
XR_001747904.2:n.477+77_477+78insC
XR_949963.3:n.477+77_477+78insC
NM_016401.4:c.268+77_268+78insC MANE Select	NP_057485.2:n.268+77_268+78insC
NM_001322404.2:c.268+77_268+78insC	NP_001309333.1:n.268+77_268+78insC
NM_001322407.2:c.151+77_151+78insC	NP_001309336.1:n.151+77_151+78insC
NM_001322409.2:c.151+77_151+78insC	NP_001309338.1:n.151+77_151+78insC
NR_024597.2:n.239+4081_239+4082insC
NR_024598.2:n.239+4081_239+4082insC
NR_136324.2:n.477+77_477+78insC