Canonical Allele Identifier: CA1703612945
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145664G= , CM000669.2:g.44145664G= GRCh38
NC_000007.13:g.44185263G= , CM000669.1:g.44185263G= GRCh37
NC_000007.12:g.44151788G= NCBI36
NG_008847.1:g.48760C=
NG_008847.2:g.57507C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1084C= ENSP00000379142.4:n.*1084C=
ENST00000616242.5:c.*206C= ENSP00000482149.2:n.*206C=
ENST00000683378.1:n.312C=
ENST00000336642.9:c.120C= ENSP00000338009.5:p.Thr40=
ENST00000345378.7:c.1089C= ENSP00000223366.2:p.Thr363=
ENST00000403799.8:c.1086C= MANE Select ENSP00000384247.3:p.Thr362=
ENST00000671824.1:c.1149C= ENSP00000500264.1:p.Thr383=
ENST00000672743.1:n.98C=
ENST00000673284.1:c.1086C= ENSP00000499852.1:p.Thr362=
ENST00000336642.8:c.138C= ENSP00000338009.4:p.Thr46=
ENST00000345378.6:c.1089C= ENSP00000223366.2:p.Thr363=
ENST00000395796.7:c.1083C= ENSP00000379142.3:p.Thr361=
ENST00000403799.7:c.1086C= ENSP00000384247.3:p.Thr362=
ENST00000437084.1:c.1035C= ENSP00000402840.1:p.Thr345=
ENST00000459642.1:n.466C=
ENST00000473353.1:n.384C=
ENST00000616242.4:c.1083C= ENSP00000482149.1:p.Thr361=
NM_000162.3:c.1086C= NP_000153.1:p.Thr362=
NM_033507.1:c.1089C= NP_277042.1:p.Thr363=
NM_033508.1:c.1083C= NP_277043.1:p.Thr361=
NM_000162.4:c.1086C= NP_000153.1:p.Thr362=
NM_001354800.1:c.1086C= NP_001341729.1:p.Thr362=
NM_001354801.1:c.75C= NP_001341730.1:p.Thr25=
NM_001354802.1:c.-55C= NP_001341731.1:n.-55C=
NM_001354803.1:c.120C= NP_001341732.1:p.Thr40=
NM_033507.2:c.1089C= NP_277042.1:p.Thr363=
NM_033508.2:c.1083C= NP_277043.1:p.Thr361=
XM_024446707.1:c.-55C= XP_024302475.1:n.-55C=
NM_000162.5:c.1086C= MANE Select NP_000153.1:p.Thr362=
NM_033507.3:c.1089C= NP_277042.1:p.Thr363=
NM_033508.3:c.1083C= NP_277043.1:p.Thr361=
NM_001354803.2:c.120C= NP_001341732.1:p.Thr40=