Canonical Allele Identifier: CA1703613418
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44146388G= , CM000669.2:g.44146388G= GRCh38
NC_000007.13:g.44185987G= , CM000669.1:g.44185987G= GRCh37
NC_000007.12:g.44152512G= NCBI36
NG_008847.1:g.48036C=
NG_008847.2:g.56783C=

Transcript Alleles

HGVS Amino-acid change
ENST00000395796.8:c.*1017+75C= ENSP00000379142.4:n.*1017+75C=
ENST00000616242.5:c.*139+75C= ENSP00000482149.2:n.*139+75C=
ENST00000683378.1:n.245+75C=
ENST00000345378.7:c.1022+75C= ENSP00000223366.2:n.1022+75C=
ENST00000403799.8:c.1019+75C= MANE Select ENSP00000384247.3:n.1019+75C=
ENST00000671824.1:c.1082+75C= ENSP00000500264.1:n.1082+75C=
ENST00000673284.1:c.1019+75C= ENSP00000499852.1:n.1019+75C=
ENST00000345378.6:c.1022+75C= ENSP00000223366.2:n.1022+75C=
ENST00000395796.7:c.1016+75C= ENSP00000379142.3:n.1016+75C=
ENST00000403799.7:c.1019+75C= ENSP00000384247.3:n.1019+75C=
ENST00000437084.1:c.968+75C= ENSP00000402840.1:n.968+75C=
ENST00000473353.1:n.317+75C=
ENST00000616242.4:c.1016+75C= ENSP00000482149.1:n.1016+75C=
NM_000162.3:c.1019+75C= NP_000153.1:n.1019+75C=
NM_033507.1:c.1022+75C= NP_277042.1:n.1022+75C=
NM_033508.1:c.1016+75C= NP_277043.1:n.1016+75C=
NM_000162.4:c.1019+75C= NP_000153.1:n.1019+75C=
NM_001354800.1:c.1019+75C= NP_001341729.1:n.1019+75C=
NM_001354801.1:c.8+231C= NP_001341730.1:n.8+231C=
NM_033507.2:c.1022+75C= NP_277042.1:n.1022+75C=
NM_033508.2:c.1016+75C= NP_277043.1:n.1016+75C=
NM_000162.5:c.1019+75C= MANE Select NP_000153.1:n.1019+75C=
NM_033507.3:c.1022+75C= NP_277042.1:n.1022+75C=
NM_033508.3:c.1016+75C= NP_277043.1:n.1016+75C=