Canonical Allele Identifier: CA367399388
Gene: GCK HGNC NCBI

Linked Data

gnomAD v4: 7-44145725-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145725G>A , CM000669.2:g.44145725G>A GRCh38
NC_000007.13:g.44185324G>A , CM000669.1:g.44185324G>A GRCh37
NC_000007.12:g.44151849G>A NCBI36
NG_008847.1:g.48699C>T
NG_008847.2:g.57446C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1023C>T ENSP00000379142.4:n.*1023C>T
ENST00000616242.5:c.*145C>T ENSP00000482149.2:n.*145C>T
ENST00000683378.1:n.251C>T
ENST00000336642.9:c.59C>T ENSP00000338009.5:p.Thr20Met
ENST00000345378.7:c.1028C>T ENSP00000223366.2:p.Thr343Met
ENST00000403799.8:c.1025C>T MANE Select ENSP00000384247.3:p.Thr342Met
ENST00000671824.1:c.1088C>T ENSP00000500264.1:p.Thr363Met
ENST00000672743.1:n.37C>T
ENST00000673284.1:c.1025C>T ENSP00000499852.1:p.Thr342Met
ENST00000336642.8:c.77C>T ENSP00000338009.4:p.Thr26Met
ENST00000345378.6:c.1028C>T ENSP00000223366.2:p.Thr343Met
ENST00000395796.7:c.1022C>T ENSP00000379142.3:p.Thr341Met
ENST00000403799.7:c.1025C>T ENSP00000384247.3:p.Thr342Met
ENST00000437084.1:c.974C>T ENSP00000402840.1:p.Thr325Met
ENST00000459642.1:n.405C>T
ENST00000473353.1:n.323C>T
ENST00000616242.4:c.1022C>T ENSP00000482149.1:p.Thr341Met
NM_000162.3:c.1025C>T NP_000153.1:p.Thr342Met
NM_033507.1:c.1028C>T NP_277042.1:p.Thr343Met
NM_033508.1:c.1022C>T NP_277043.1:p.Thr341Met
NM_000162.4:c.1025C>T NP_000153.1:p.Thr342Met
NM_001354800.1:c.1025C>T NP_001341729.1:p.Thr342Met
NM_001354801.1:c.14C>T NP_001341730.1:p.Thr5Met
NM_001354802.1:c.-116C>T NP_001341731.1:n.-116C>T
NM_001354803.1:c.59C>T NP_001341732.1:p.Thr20Met
NM_033507.2:c.1028C>T NP_277042.1:p.Thr343Met
NM_033508.2:c.1022C>T NP_277043.1:p.Thr341Met
XM_024446707.1:c.-116C>T XP_024302475.1:n.-116C>T
NM_000162.5:c.1025C>T MANE Select NP_000153.1:p.Thr342Met
NM_033507.3:c.1028C>T NP_277042.1:p.Thr343Met
NM_033508.3:c.1022C>T NP_277043.1:p.Thr341Met
NM_001354803.2:c.59C>T NP_001341732.1:p.Thr20Met