Canonical Allele Identifier: CA346158064
Gene: KHK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27092334G>A , CM000664.2:g.27092334G>A GRCh38
NC_000002.11:g.27315202G>A , CM000664.1:g.27315202G>A GRCh37
NC_000002.10:g.27168706G>A NCBI36
NG_012199.1:g.10592G>A
NG_012199.2:g.10592G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260599.11:c.95G>A ENSP00000260599.6:p.Cys32Tyr
ENST00000429697.2:c.95G>A ENSP00000404741.2:p.Cys32Tyr
ENST00000260598.10:c.95G>A MANE Select ENSP00000260598.5:p.Cys32Tyr
ENST00000260598.9:c.95G>A ENSP00000260598.5:p.Cys32Tyr
ENST00000260599.10:c.95G>A ENSP00000260599.6:p.Cys32Tyr
ENST00000429697.1:c.95G>A ENSP00000404741.1:p.Cys32Tyr
ENST00000490823.5:n.443G>A
NM_000221.2:c.95G>A NP_000212.1:p.Cys32Tyr
NM_006488.2:c.95G>A NP_006479.1:p.Cys32Tyr
XM_005264294.2:c.95G>A XP_005264351.1:p.Cys32Tyr
XM_005264296.2:c.95G>A XP_005264353.1:p.Cys32Tyr
XM_005264298.2:c.93-4395G>A XP_005264355.1:n.93-4395G>A
XM_006712008.2:c.95G>A XP_006712071.1:p.Cys32Tyr
XM_006712009.2:c.95G>A XP_006712072.1:p.Cys32Tyr
XM_006712010.2:c.95G>A XP_006712073.1:p.Cys32Tyr
XM_006712011.2:c.95G>A XP_006712074.1:p.Cys32Tyr
XM_006712012.2:c.95G>A XP_006712075.1:p.Cys32Tyr
XM_006712013.2:c.95G>A XP_006712076.1:p.Cys32Tyr
XM_006712014.2:c.93-4395G>A XP_006712077.1:n.93-4395G>A
XM_005264294.4:c.95G>A XP_005264351.1:p.Cys32Tyr
XM_005264296.4:c.95G>A XP_005264353.1:p.Cys32Tyr
XM_005264298.4:c.93-4395G>A XP_005264355.1:n.93-4395G>A
XM_006712008.4:c.95G>A XP_006712071.1:p.Cys32Tyr
XM_006712009.4:c.95G>A XP_006712072.1:p.Cys32Tyr
XM_006712010.4:c.95G>A XP_006712073.1:p.Cys32Tyr
XM_006712011.4:c.95G>A XP_006712074.1:p.Cys32Tyr
XM_006712012.4:c.95G>A XP_006712075.1:p.Cys32Tyr
XM_006712013.4:c.95G>A XP_006712076.1:p.Cys32Tyr
XM_006712014.4:c.93-4395G>A XP_006712077.1:n.93-4395G>A
XM_017004060.2:c.95G>A XP_016859549.1:p.Cys32Tyr
XM_017004061.2:c.95G>A XP_016859550.1:p.Cys32Tyr
NM_006488.3:c.95G>A MANE Select NP_006479.1:p.Cys32Tyr
NM_000221.3:c.95G>A NP_000212.1:p.Cys32Tyr