Canonical Allele Identifier: CA367399292
Gene: GCK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145706G>C , CM000669.2:g.44145706G>C GRCh38
NC_000007.13:g.44185305G>C , CM000669.1:g.44185305G>C GRCh37
NC_000007.12:g.44151830G>C NCBI36
NG_008847.1:g.48718C>G
NG_008847.2:g.57465C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1042C>G ENSP00000379142.4:n.*1042C>G
ENST00000616242.5:c.*164C>G ENSP00000482149.2:n.*164C>G
ENST00000683378.1:n.270C>G
ENST00000336642.9:c.78C>G ENSP00000338009.5:p.Ile26Met
ENST00000345378.7:c.1047C>G ENSP00000223366.2:p.Ile349Met
ENST00000403799.8:c.1044C>G MANE Select ENSP00000384247.3:p.Ile348Met
ENST00000671824.1:c.1107C>G ENSP00000500264.1:p.Ile369Met
ENST00000672743.1:n.56C>G
ENST00000673284.1:c.1044C>G ENSP00000499852.1:p.Ile348Met
ENST00000336642.8:c.96C>G ENSP00000338009.4:p.Ile32Met
ENST00000345378.6:c.1047C>G ENSP00000223366.2:p.Ile349Met
ENST00000395796.7:c.1041C>G ENSP00000379142.3:p.Ile347Met
ENST00000403799.7:c.1044C>G ENSP00000384247.3:p.Ile348Met
ENST00000437084.1:c.993C>G ENSP00000402840.1:p.Ile331Met
ENST00000459642.1:n.424C>G
ENST00000473353.1:n.342C>G
ENST00000616242.4:c.1041C>G ENSP00000482149.1:p.Ile347Met
NM_000162.3:c.1044C>G NP_000153.1:p.Ile348Met
NM_033507.1:c.1047C>G NP_277042.1:p.Ile349Met
NM_033508.1:c.1041C>G NP_277043.1:p.Ile347Met
NM_000162.4:c.1044C>G NP_000153.1:p.Ile348Met
NM_001354800.1:c.1044C>G NP_001341729.1:p.Ile348Met
NM_001354801.1:c.33C>G NP_001341730.1:p.Ile11Met
NM_001354802.1:c.-97C>G NP_001341731.1:n.-97C>G
NM_001354803.1:c.78C>G NP_001341732.1:p.Ile26Met
NM_033507.2:c.1047C>G NP_277042.1:p.Ile349Met
NM_033508.2:c.1041C>G NP_277043.1:p.Ile347Met
XM_024446707.1:c.-97C>G XP_024302475.1:n.-97C>G
NM_000162.5:c.1044C>G MANE Select NP_000153.1:p.Ile348Met
NM_033507.3:c.1047C>G NP_277042.1:p.Ile349Met
NM_033508.3:c.1041C>G NP_277043.1:p.Ile347Met
NM_001354803.2:c.78C>G NP_001341732.1:p.Ile26Met