Canonical Allele Identifier: CA367398738
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3024419
ClinVar RCV Id: RCV003883455

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145603A>T , CM000669.2:g.44145603A>T GRCh38
NC_000007.13:g.44185202A>T , CM000669.1:g.44185202A>T GRCh37
NC_000007.12:g.44151727A>T NCBI36
NG_008847.1:g.48821T>A
NG_008847.2:g.57568T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1145T>A ENSP00000379142.4:n.*1145T>A
ENST00000616242.5:c.*267T>A ENSP00000482149.2:n.*267T>A
ENST00000683378.1:n.373T>A
ENST00000336642.9:c.181T>A ENSP00000338009.5:p.Ser61Thr
ENST00000345378.7:c.1150T>A ENSP00000223366.2:p.Ser384Thr
ENST00000403799.8:c.1147T>A MANE Select ENSP00000384247.3:p.Ser383Thr
ENST00000671824.1:c.1210T>A ENSP00000500264.1:p.Ser404Thr
ENST00000672743.1:n.159T>A
ENST00000673284.1:c.1147T>A ENSP00000499852.1:p.Ser383Thr
ENST00000336642.8:c.199T>A ENSP00000338009.4:p.Ser67Thr
ENST00000345378.6:c.1150T>A ENSP00000223366.2:p.Ser384Thr
ENST00000395796.7:c.1144T>A ENSP00000379142.3:p.Ser382Thr
ENST00000403799.7:c.1147T>A ENSP00000384247.3:p.Ser383Thr
ENST00000437084.1:c.1096T>A ENSP00000402840.1:p.Ser366Thr
ENST00000459642.1:n.527T>A
ENST00000616242.4:c.1144T>A ENSP00000482149.1:p.Ser382Thr
NM_000162.3:c.1147T>A NP_000153.1:p.Ser383Thr
NM_033507.1:c.1150T>A NP_277042.1:p.Ser384Thr
NM_033508.1:c.1144T>A NP_277043.1:p.Ser382Thr
NM_000162.4:c.1147T>A NP_000153.1:p.Ser383Thr
NM_001354800.1:c.1147T>A NP_001341729.1:p.Ser383Thr
NM_001354801.1:c.136T>A NP_001341730.1:p.Ser46Thr
NM_001354802.1:c.7T>A NP_001341731.1:p.Ser3Thr
NM_001354803.1:c.181T>A NP_001341732.1:p.Ser61Thr
NM_033507.2:c.1150T>A NP_277042.1:p.Ser384Thr
NM_033508.2:c.1144T>A NP_277043.1:p.Ser382Thr
XM_024446707.1:c.7T>A XP_024302475.1:p.Ser3Thr
NM_000162.5:c.1147T>A MANE Select NP_000153.1:p.Ser383Thr
NM_033507.3:c.1150T>A NP_277042.1:p.Ser384Thr
NM_033508.3:c.1144T>A NP_277043.1:p.Ser382Thr
NM_001354803.2:c.181T>A NP_001341732.1:p.Ser61Thr