Canonical Allele Identifier: CA367398797
Gene: GCK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145615C>G , CM000669.2:g.44145615C>G GRCh38
NC_000007.13:g.44185214C>G , CM000669.1:g.44185214C>G GRCh37
NC_000007.12:g.44151739C>G NCBI36
NG_008847.1:g.48809G>C
NG_008847.2:g.57556G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1133G>C ENSP00000379142.4:n.*1133G>C
ENST00000616242.5:c.*255G>C ENSP00000482149.2:n.*255G>C
ENST00000683378.1:n.361G>C
ENST00000336642.9:c.169G>C ENSP00000338009.5:p.Ala57Pro
ENST00000345378.7:c.1138G>C ENSP00000223366.2:p.Ala380Pro
ENST00000403799.8:c.1135G>C MANE Select ENSP00000384247.3:p.Ala379Pro
ENST00000671824.1:c.1198G>C ENSP00000500264.1:p.Ala400Pro
ENST00000672743.1:n.147G>C
ENST00000673284.1:c.1135G>C ENSP00000499852.1:p.Ala379Pro
ENST00000336642.8:c.187G>C ENSP00000338009.4:p.Ala63Pro
ENST00000345378.6:c.1138G>C ENSP00000223366.2:p.Ala380Pro
ENST00000395796.7:c.1132G>C ENSP00000379142.3:p.Ala378Pro
ENST00000403799.7:c.1135G>C ENSP00000384247.3:p.Ala379Pro
ENST00000437084.1:c.1084G>C ENSP00000402840.1:p.Ala362Pro
ENST00000459642.1:n.515G>C
ENST00000616242.4:c.1132G>C ENSP00000482149.1:p.Ala378Pro
NM_000162.3:c.1135G>C NP_000153.1:p.Ala379Pro
NM_033507.1:c.1138G>C NP_277042.1:p.Ala380Pro
NM_033508.1:c.1132G>C NP_277043.1:p.Ala378Pro
NM_000162.4:c.1135G>C NP_000153.1:p.Ala379Pro
NM_001354800.1:c.1135G>C NP_001341729.1:p.Ala379Pro
NM_001354801.1:c.124G>C NP_001341730.1:p.Ala42Pro
NM_001354802.1:c.-6G>C NP_001341731.1:n.-6G>C
NM_001354803.1:c.169G>C NP_001341732.1:p.Ala57Pro
NM_033507.2:c.1138G>C NP_277042.1:p.Ala380Pro
NM_033508.2:c.1132G>C NP_277043.1:p.Ala378Pro
XM_024446707.1:c.-6G>C XP_024302475.1:n.-6G>C
NM_000162.5:c.1135G>C MANE Select NP_000153.1:p.Ala379Pro
NM_033507.3:c.1138G>C NP_277042.1:p.Ala380Pro
NM_033508.3:c.1132G>C NP_277043.1:p.Ala378Pro
NM_001354803.2:c.169G>C NP_001341732.1:p.Ala57Pro