Canonical Allele Identifier: CA1703634744
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44147418_44147422delinsCGGAA , CM000669.2:g.44147418_44147422delinsCGGAA GRCh38
NC_000007.13:g.44187017_44187021delinsCGGAA , CM000669.1:g.44187017_44187021delinsCGGAA GRCh37
NC_000007.12:g.44153542_44153546delinsCGGAA NCBI36
NG_008847.1:g.47002_47006delinsTTCCG
NG_008847.2:g.55749_55753delinsTTCCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*861+228_*861+232delinsTTCCG ENSP00000379142.4:n.*861+228_*861+232delinsTTCCG
ENST00000616242.5:c.853+238_853+242delinsTTCCG ENSP00000482149.2:n.853+238_853+242delinsTTCCG
ENST00000345378.7:c.866+228_866+232delinsTTCCG ENSP00000223366.2:n.866+228_866+232delinsTTCCG
ENST00000403799.8:c.863+228_863+232delinsTTCCG MANE Select ENSP00000384247.3:n.863+228_863+232delinsTTCCG
ENST00000671824.1:c.854-9_854-5delinsTTCCG ENSP00000500264.1:n.854-9_854-5delinsTTCCG
ENST00000673284.1:c.863+228_863+232delinsTTCCG ENSP00000499852.1:n.863+228_863+232delinsTTCCG
ENST00000345378.6:c.866+228_866+232delinsTTCCG ENSP00000223366.2:n.866+228_866+232delinsTTCCG
ENST00000395796.7:c.860+228_860+232delinsTTCCG ENSP00000379142.3:n.860+228_860+232delinsTTCCG
ENST00000403799.7:c.863+228_863+232delinsTTCCG ENSP00000384247.3:n.863+228_863+232delinsTTCCG
ENST00000437084.1:c.812+228_812+232delinsTTCCG ENSP00000402840.1:n.812+228_812+232delinsTTCCG
ENST00000616242.4:c.860+228_860+232delinsTTCCG ENSP00000482149.1:n.860+228_860+232delinsTTCCG
NM_000162.3:c.863+228_863+232delinsTTCCG NP_000153.1:n.863+228_863+232delinsTTCCG
NM_033507.1:c.866+228_866+232delinsTTCCG NP_277042.1:n.866+228_866+232delinsTTCCG
NM_033508.1:c.860+228_860+232delinsTTCCG NP_277043.1:n.860+228_860+232delinsTTCCG
NM_000162.4:c.863+228_863+232delinsTTCCG NP_000153.1:n.863+228_863+232delinsTTCCG
NM_001354800.1:c.863+228_863+232delinsTTCCG NP_001341729.1:n.863+228_863+232delinsTTCCG
NM_033507.2:c.866+228_866+232delinsTTCCG NP_277042.1:n.866+228_866+232delinsTTCCG
NM_033508.2:c.860+228_860+232delinsTTCCG NP_277043.1:n.860+228_860+232delinsTTCCG
NM_000162.5:c.863+228_863+232delinsTTCCG MANE Select NP_000153.1:n.863+228_863+232delinsTTCCG
NM_033507.3:c.866+228_866+232delinsTTCCG NP_277042.1:n.866+228_866+232delinsTTCCG
NM_033508.3:c.860+228_860+232delinsTTCCG NP_277043.1:n.860+228_860+232delinsTTCCG