Canonical Allele Identifier: CA2523278877

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44152571_44152572insG , CM000669.2:g.44152571_44152572insG	GRCh38
NC_000007.13:g.44192170_44192171insG , CM000669.1:g.44192170_44192171insG	GRCh37
NC_000007.12:g.44158695_44158696insG	NCBI36
NG_008847.1:g.41852_41853insC
NG_008847.2:g.50599_50600insC

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*207-147_*207-146insC	ENSP00000379142.4:n.*207-147_*207-146insC...
ENST00000616242.5:c.209-147_209-146insC	ENSP00000482149.2:n.209-147_209-146insC
ENST00000682635.1:n.695-147_695-146insC
ENST00000345378.7:c.212-147_212-146insC	ENSP00000223366.2:n.212-147_212-146insC
ENST00000403799.8:c.209-147_209-146insC MANE Select	ENSP00000384247.3:n.209-147_209-146insC
ENST00000671824.1:c.209-147_209-146insC	ENSP00000500264.1:n.209-147_209-146insC
ENST00000673284.1:c.209-147_209-146insC	ENSP00000499852.1:n.209-147_209-146insC
ENST00000345378.6:c.212-147_212-146insC	ENSP00000223366.2:n.212-147_212-146insC
ENST00000395796.7:c.206-147_206-146insC	ENSP00000379142.3:n.206-147_206-146insC
ENST00000403799.7:c.209-147_209-146insC	ENSP00000384247.3:n.209-147_209-146insC
ENST00000437084.1:c.209-147_209-146insC	ENSP00000402840.1:n.209-147_209-146insC
ENST00000616242.4:c.206-147_206-146insC	ENSP00000482149.1:n.206-147_206-146insC
NM_000162.3:c.209-147_209-146insC	NP_000153.1:n.209-147_209-146insC
NM_033507.1:c.212-147_212-146insC	NP_277042.1:n.212-147_212-146insC
NM_033508.1:c.206-147_206-146insC	NP_277043.1:n.206-147_206-146insC
NM_000162.4:c.209-147_209-146insC	NP_000153.1:n.209-147_209-146insC
NM_001354800.1:c.209-147_209-146insC	NP_001341729.1:n.209-147_209-146insC
NM_033507.2:c.212-147_212-146insC	NP_277042.1:n.212-147_212-146insC
NM_033508.2:c.206-147_206-146insC	NP_277043.1:n.206-147_206-146insC
NM_000162.5:c.209-147_209-146insC MANE Select	NP_000153.1:n.209-147_209-146insC
NM_033507.3:c.212-147_212-146insC	NP_277042.1:n.212-147_212-146insC
NM_033508.3:c.206-147_206-146insC	NP_277043.1:n.206-147_206-146insC