Canonical Allele Identifier: CA2695203019

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44153339_44153340delinsC , CM000669.2:g.44153339_44153340delinsC	GRCh38
NC_000007.13:g.44192938_44192939delinsC , CM000669.1:g.44192938_44192939delinsC	GRCh37
NC_000007.12:g.44159463_44159464delinsC	NCBI36
NG_008847.1:g.41084_41085delinsG
NG_008847.2:g.49831_49832delinsG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*167_*168delinsG	ENSP00000379142.4:n.*167_*168delinsG
ENST00000616242.5:c.169_170delinsG	ENSP00000482149.2:p.Met57GlyfsTer30
ENST00000682635.1:n.655_656delinsG
ENST00000345378.7:c.172_173delinsG	ENSP00000223366.2:p.Met58GlyfsTer30
ENST00000403799.8:c.169_170delinsG MANE Select	ENSP00000384247.3:p.Met57GlyfsTer30
ENST00000671824.1:c.169_170delinsG	ENSP00000500264.1:p.Met57GlyfsTer30
ENST00000673284.1:c.169_170delinsG	ENSP00000499852.1:p.Met57GlyfsTer30
ENST00000345378.6:c.172_173delinsG	ENSP00000223366.2:p.Met58GlyfsTer30
ENST00000395796.7:c.166_167delinsG	ENSP00000379142.3:p.Met56GlyfsTer30
ENST00000403799.7:c.169_170delinsG	ENSP00000384247.3:p.Met57GlyfsTer30
ENST00000437084.1:c.169_170delinsG	ENSP00000402840.1:p.Met57GlyfsTer30
ENST00000616242.4:c.166_167delinsG	ENSP00000482149.1:p.Met56GlyfsTer30
NM_000162.3:c.169_170delinsG	NP_000153.1:p.Met57GlyfsTer30
NM_033507.1:c.172_173delinsG	NP_277042.1:p.Met58GlyfsTer30
NM_033508.1:c.166_167delinsG	NP_277043.1:p.Met56GlyfsTer30
NM_000162.4:c.169_170delinsG	NP_000153.1:p.Met57GlyfsTer30
NM_001354800.1:c.169_170delinsG	NP_001341729.1:p.Met57GlyfsTer30
NM_033507.2:c.172_173delinsG	NP_277042.1:p.Met58GlyfsTer30
NM_033508.2:c.166_167delinsG	NP_277043.1:p.Met56GlyfsTer30
NM_000162.5:c.169_170delinsG MANE Select	NP_000153.1:p.Met57GlyfsTer30
NM_033507.3:c.172_173delinsG	NP_277042.1:p.Met58GlyfsTer30
NM_033508.3:c.166_167delinsG	NP_277043.1:p.Met56GlyfsTer30