Canonical Allele Identifier: CA367399134
Gene: GCK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145675G>C , CM000669.2:g.44145675G>C GRCh38
NC_000007.13:g.44185274G>C , CM000669.1:g.44185274G>C GRCh37
NC_000007.12:g.44151799G>C NCBI36
NG_008847.1:g.48749C>G
NG_008847.2:g.57496C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1073C>G ENSP00000379142.4:n.*1073C>G
ENST00000616242.5:c.*195C>G ENSP00000482149.2:n.*195C>G
ENST00000683378.1:n.301C>G
ENST00000336642.9:c.109C>G ENSP00000338009.5:p.Pro37Ala
ENST00000345378.7:c.1078C>G ENSP00000223366.2:p.Pro360Ala
ENST00000403799.8:c.1075C>G MANE Select ENSP00000384247.3:p.Pro359Ala
ENST00000671824.1:c.1138C>G ENSP00000500264.1:p.Pro380Ala
ENST00000672743.1:n.87C>G
ENST00000673284.1:c.1075C>G ENSP00000499852.1:p.Pro359Ala
ENST00000336642.8:c.127C>G ENSP00000338009.4:p.Pro43Ala
ENST00000345378.6:c.1078C>G ENSP00000223366.2:p.Pro360Ala
ENST00000395796.7:c.1072C>G ENSP00000379142.3:p.Pro358Ala
ENST00000403799.7:c.1075C>G ENSP00000384247.3:p.Pro359Ala
ENST00000437084.1:c.1024C>G ENSP00000402840.1:p.Pro342Ala
ENST00000459642.1:n.455C>G
ENST00000473353.1:n.373C>G
ENST00000616242.4:c.1072C>G ENSP00000482149.1:p.Pro358Ala
NM_000162.3:c.1075C>G NP_000153.1:p.Pro359Ala
NM_033507.1:c.1078C>G NP_277042.1:p.Pro360Ala
NM_033508.1:c.1072C>G NP_277043.1:p.Pro358Ala
NM_000162.4:c.1075C>G NP_000153.1:p.Pro359Ala
NM_001354800.1:c.1075C>G NP_001341729.1:p.Pro359Ala
NM_001354801.1:c.64C>G NP_001341730.1:p.Pro22Ala
NM_001354802.1:c.-66C>G NP_001341731.1:n.-66C>G
NM_001354803.1:c.109C>G NP_001341732.1:p.Pro37Ala
NM_033507.2:c.1078C>G NP_277042.1:p.Pro360Ala
NM_033508.2:c.1072C>G NP_277043.1:p.Pro358Ala
XM_024446707.1:c.-66C>G XP_024302475.1:n.-66C>G
NM_000162.5:c.1075C>G MANE Select NP_000153.1:p.Pro359Ala
NM_033507.3:c.1078C>G NP_277042.1:p.Pro360Ala
NM_033508.3:c.1072C>G NP_277043.1:p.Pro358Ala
NM_001354803.2:c.109C>G NP_001341732.1:p.Pro37Ala