Canonical Allele Identifier: CA2658288213

Gene: KHK

Linked Data

• gnomAD v4: 2-27092180-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27092180C>A , CM000664.2:g.27092180C>A	GRCh38
NC_000002.11:g.27315048C>A , CM000664.1:g.27315048C>A	GRCh37
NC_000002.10:g.27168552C>A	NCBI36
NG_012199.1:g.10438C>A
NG_012199.2:g.10438C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260599.11:c.93-152C>A	ENSP00000260599.6:n.93-152C>A
ENST00000429697.2:c.93-152C>A	ENSP00000404741.2:n.93-152C>A
ENST00000260598.10:c.93-152C>A MANE Select	ENSP00000260598.5:n.93-152C>A
ENST00000260598.9:c.93-152C>A	ENSP00000260598.5:n.93-152C>A
ENST00000260599.10:c.93-152C>A	ENSP00000260599.6:n.93-152C>A
ENST00000429697.1:c.93-152C>A	ENSP00000404741.1:n.93-152C>A
ENST00000490823.5:n.441-152C>A
NM_000221.2:c.93-152C>A	NP_000212.1:n.93-152C>A
NM_006488.2:c.93-152C>A	NP_006479.1:n.93-152C>A
XM_005264294.2:c.93-152C>A	XP_005264351.1:n.93-152C>A
XM_005264296.2:c.93-152C>A	XP_005264353.1:n.93-152C>A
XM_005264298.2:c.93-4549C>A	XP_005264355.1:n.93-4549C>A
XM_006712008.2:c.93-152C>A	XP_006712071.1:n.93-152C>A
XM_006712009.2:c.93-152C>A	XP_006712072.1:n.93-152C>A
XM_006712010.2:c.93-152C>A	XP_006712073.1:n.93-152C>A
XM_006712011.2:c.93-152C>A	XP_006712074.1:n.93-152C>A
XM_006712012.2:c.93-152C>A	XP_006712075.1:n.93-152C>A
XM_006712013.2:c.93-152C>A	XP_006712076.1:n.93-152C>A
XM_006712014.2:c.93-4549C>A	XP_006712077.1:n.93-4549C>A
XM_005264294.4:c.93-152C>A	XP_005264351.1:n.93-152C>A
XM_005264296.4:c.93-152C>A	XP_005264353.1:n.93-152C>A
XM_005264298.4:c.93-4549C>A	XP_005264355.1:n.93-4549C>A
XM_006712008.4:c.93-152C>A	XP_006712071.1:n.93-152C>A
XM_006712009.4:c.93-152C>A	XP_006712072.1:n.93-152C>A
XM_006712010.4:c.93-152C>A	XP_006712073.1:n.93-152C>A
XM_006712011.4:c.93-152C>A	XP_006712074.1:n.93-152C>A
XM_006712012.4:c.93-152C>A	XP_006712075.1:n.93-152C>A
XM_006712013.4:c.93-152C>A	XP_006712076.1:n.93-152C>A
XM_006712014.4:c.93-4549C>A	XP_006712077.1:n.93-4549C>A
XM_017004060.2:c.93-152C>A	XP_016859549.1:n.93-152C>A
XM_017004061.2:c.93-152C>A	XP_016859550.1:n.93-152C>A
NM_006488.3:c.93-152C>A MANE Select	NP_006479.1:n.93-152C>A
NM_000221.3:c.93-152C>A	NP_000212.1:n.93-152C>A