Canonical Allele Identifier: CA1703637178
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44152613_44152614delinsAG , CM000669.2:g.44152613_44152614delinsAG GRCh38
NC_000007.13:g.44192212_44192213delinsAG , CM000669.1:g.44192212_44192213delinsAG GRCh37
NC_000007.12:g.44158737_44158738delinsAG NCBI36
NG_008847.1:g.41810_41811delinsCT
NG_008847.2:g.50557_50558delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000395796.8:c.*207-189_*207-188delinsCT ENSP00000379142.4:n.*207-189_*207-188delinsCT
ENST00000616242.5:c.209-189_209-188delinsCT ENSP00000482149.2:n.209-189_209-188delinsCT
ENST00000682635.1:n.695-189_695-188delinsCT
ENST00000345378.7:c.212-189_212-188delinsCT ENSP00000223366.2:n.212-189_212-188delinsCT
ENST00000403799.8:c.209-189_209-188delinsCT MANE Select ENSP00000384247.3:n.209-189_209-188delinsCT
ENST00000671824.1:c.209-189_209-188delinsCT ENSP00000500264.1:n.209-189_209-188delinsCT
ENST00000673284.1:c.209-189_209-188delinsCT ENSP00000499852.1:n.209-189_209-188delinsCT
ENST00000345378.6:c.212-189_212-188delinsCT ENSP00000223366.2:n.212-189_212-188delinsCT
ENST00000395796.7:c.206-189_206-188delinsCT ENSP00000379142.3:n.206-189_206-188delinsCT
ENST00000403799.7:c.209-189_209-188delinsCT ENSP00000384247.3:n.209-189_209-188delinsCT
ENST00000437084.1:c.209-189_209-188delinsCT ENSP00000402840.1:n.209-189_209-188delinsCT
ENST00000616242.4:c.206-189_206-188delinsCT ENSP00000482149.1:n.206-189_206-188delinsCT
NM_000162.3:c.209-189_209-188delinsCT NP_000153.1:n.209-189_209-188delinsCT
NM_033507.1:c.212-189_212-188delinsCT NP_277042.1:n.212-189_212-188delinsCT
NM_033508.1:c.206-189_206-188delinsCT NP_277043.1:n.206-189_206-188delinsCT
NM_000162.4:c.209-189_209-188delinsCT NP_000153.1:n.209-189_209-188delinsCT
NM_001354800.1:c.209-189_209-188delinsCT NP_001341729.1:n.209-189_209-188delinsCT
NM_033507.2:c.212-189_212-188delinsCT NP_277042.1:n.212-189_212-188delinsCT
NM_033508.2:c.206-189_206-188delinsCT NP_277043.1:n.206-189_206-188delinsCT
NM_000162.5:c.209-189_209-188delinsCT MANE Select NP_000153.1:n.209-189_209-188delinsCT
NM_033507.3:c.212-189_212-188delinsCT NP_277042.1:n.212-189_212-188delinsCT
NM_033508.3:c.206-189_206-188delinsCT NP_277043.1:n.206-189_206-188delinsCT