Canonical Allele Identifier: CA767299681
Gene: KHK HGNC NCBI

Linked Data

dbSNP Id: rs1453239142
gnomAD v3: 2-27092113-T-C
gnomAD v4: 2-27092113-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27092113T>C , CM000664.2:g.27092113T>C GRCh38
NC_000002.11:g.27314981T>C , CM000664.1:g.27314981T>C GRCh37
NC_000002.10:g.27168485T>C NCBI36
NG_012199.1:g.10371T>C
NG_012199.2:g.10371T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260599.11:c.93-219T>C ENSP00000260599.6:n.93-219T>C
ENST00000429697.2:c.93-219T>C ENSP00000404741.2:n.93-219T>C
ENST00000260598.10:c.93-219T>C MANE Select ENSP00000260598.5:n.93-219T>C
ENST00000260598.9:c.93-219T>C ENSP00000260598.5:n.93-219T>C
ENST00000260599.10:c.93-219T>C ENSP00000260599.6:n.93-219T>C
ENST00000429697.1:c.93-219T>C ENSP00000404741.1:n.93-219T>C
ENST00000490823.5:n.441-219T>C
NM_000221.2:c.93-219T>C NP_000212.1:n.93-219T>C
NM_006488.2:c.93-219T>C NP_006479.1:n.93-219T>C
XM_005264294.2:c.93-219T>C XP_005264351.1:n.93-219T>C
XM_005264296.2:c.93-219T>C XP_005264353.1:n.93-219T>C
XM_005264298.2:c.93-4616T>C XP_005264355.1:n.93-4616T>C
XM_006712008.2:c.93-219T>C XP_006712071.1:n.93-219T>C
XM_006712009.2:c.93-219T>C XP_006712072.1:n.93-219T>C
XM_006712010.2:c.93-219T>C XP_006712073.1:n.93-219T>C
XM_006712011.2:c.93-219T>C XP_006712074.1:n.93-219T>C
XM_006712012.2:c.93-219T>C XP_006712075.1:n.93-219T>C
XM_006712013.2:c.93-219T>C XP_006712076.1:n.93-219T>C
XM_006712014.2:c.93-4616T>C XP_006712077.1:n.93-4616T>C
XM_005264294.4:c.93-219T>C XP_005264351.1:n.93-219T>C
XM_005264296.4:c.93-219T>C XP_005264353.1:n.93-219T>C
XM_005264298.4:c.93-4616T>C XP_005264355.1:n.93-4616T>C
XM_006712008.4:c.93-219T>C XP_006712071.1:n.93-219T>C
XM_006712009.4:c.93-219T>C XP_006712072.1:n.93-219T>C
XM_006712010.4:c.93-219T>C XP_006712073.1:n.93-219T>C
XM_006712011.4:c.93-219T>C XP_006712074.1:n.93-219T>C
XM_006712012.4:c.93-219T>C XP_006712075.1:n.93-219T>C
XM_006712013.4:c.93-219T>C XP_006712076.1:n.93-219T>C
XM_006712014.4:c.93-4616T>C XP_006712077.1:n.93-4616T>C
XM_017004060.2:c.93-219T>C XP_016859549.1:n.93-219T>C
XM_017004061.2:c.93-219T>C XP_016859550.1:n.93-219T>C
NM_006488.3:c.93-219T>C MANE Select NP_006479.1:n.93-219T>C
NM_000221.3:c.93-219T>C NP_000212.1:n.93-219T>C