Canonical Allele Identifier: CA382016709

Gene: HIKESHI

Linked Data

• gnomAD v4: 11-86306303-A-G
• MyVariant Identifiers: chr11:g.86017345A>G (hg19) ; chr11:g.86306303A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.86306303A>G , CM000673.2:g.86306303A>G	GRCh38
NC_000011.9:g.86017345A>G , CM000673.1:g.86017345A>G	GRCh37
NC_000011.8:g.85694993A>G	NCBI36
NG_046865.1:g.9093A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278483.8:c.89A>G MANE Select	ENSP00000278483.3:p.Tyr30Cys
ENST00000278483.7:c.89A>G	ENSP00000278483.3:p.Tyr30Cys
ENST00000528004.5:c.89A>G	ENSP00000433815.1:p.Tyr30Cys
ENST00000530208.1:n.164A>G
ENST00000531485.5:n.236+3825A>G
ENST00000532270.5:n.428A>G
ENST00000533986.5:c.89A>G	ENSP00000432699.1:p.Tyr30Cys
NM_016401.3:c.89A>G	NP_057485.2:p.Tyr30Cys
NR_024596.1:n.164A>G
NR_024597.1:n.268+3825A>G
NR_024598.1:n.268+3825A>G
XM_011545097.1:c.-29A>G	XP_011543399.1:n.-29A>G
XR_949963.1:n.312A>G
NM_001322404.1:c.89A>G	NP_001309333.1:p.Tyr30Cys
NM_001322407.1:c.-29A>G	NP_001309336.1:n.-29A>G
NM_001322409.1:c.-29A>G	NP_001309338.1:n.-29A>G
NR_136324.1:n.311A>G
XM_017017914.2:c.89A>G	XP_016873403.1:p.Tyr30Cys
XM_017017915.1:c.-29A>G	XP_016873404.1:n.-29A>G
XR_001747904.2:n.298A>G
XR_949963.3:n.298A>G
NM_016401.4:c.89A>G MANE Select	NP_057485.2:p.Tyr30Cys
NM_001322404.2:c.89A>G	NP_001309333.1:p.Tyr30Cys
NM_001322407.2:c.-29A>G	NP_001309336.1:n.-29A>G
NM_001322409.2:c.-29A>G	NP_001309338.1:n.-29A>G
NR_024597.2:n.239+3825A>G
NR_024598.2:n.239+3825A>G
NR_136324.2:n.298A>G