Canonical Allele Identifier: CA651288860
Gene: GCK HGNC NCBI

Linked Data

COSMIC: COSN2224157
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44147447_44147451del , CM000669.2:g.44147447_44147451del GRCh38
NC_000007.13:g.44187046_44187050del , CM000669.1:g.44187046_44187050del GRCh37
NC_000007.12:g.44153571_44153575del NCBI36
NG_008847.1:g.46979_46983del
NG_008847.2:g.55726_55730del

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*861+205_*861+209del ENSP00000379142.4:n.*861+205_*861+209del
ENST00000616242.5:c.853+215_853+219del ENSP00000482149.2:n.853+215_853+219del
ENST00000345378.7:c.866+205_866+209del ENSP00000223366.2:n.866+205_866+209del
ENST00000403799.8:c.863+205_863+209del MANE Select ENSP00000384247.3:n.863+205_863+209del
ENST00000671824.1:c.854-32_854-28del ENSP00000500264.1:n.854-32_854-28del
ENST00000673284.1:c.863+205_863+209del ENSP00000499852.1:n.863+205_863+209del
ENST00000345378.6:c.866+205_866+209del ENSP00000223366.2:n.866+205_866+209del
ENST00000395796.7:c.860+205_860+209del ENSP00000379142.3:n.860+205_860+209del
ENST00000403799.7:c.863+205_863+209del ENSP00000384247.3:n.863+205_863+209del
ENST00000437084.1:c.812+205_812+209del ENSP00000402840.1:n.812+205_812+209del
ENST00000616242.4:c.860+205_860+209del ENSP00000482149.1:n.860+205_860+209del
NM_000162.3:c.863+205_863+209del NP_000153.1:n.863+205_863+209del
NM_033507.1:c.866+205_866+209del NP_277042.1:n.866+205_866+209del
NM_033508.1:c.860+205_860+209del NP_277043.1:n.860+205_860+209del
NM_000162.4:c.863+205_863+209del NP_000153.1:n.863+205_863+209del
NM_001354800.1:c.863+205_863+209del NP_001341729.1:n.863+205_863+209del
NM_033507.2:c.866+205_866+209del NP_277042.1:n.866+205_866+209del
NM_033508.2:c.860+205_860+209del NP_277043.1:n.860+205_860+209del
NM_000162.5:c.863+205_863+209del MANE Select NP_000153.1:n.863+205_863+209del
NM_033507.3:c.866+205_866+209del NP_277042.1:n.866+205_866+209del
NM_033508.3:c.860+205_860+209del NP_277043.1:n.860+205_860+209del
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