Canonical Allele Identifier: CA3004402153

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44149736_44149737del , CM000669.2:g.44149736_44149737del	GRCh38
NC_000007.13:g.44189335_44189336del , CM000669.1:g.44189335_44189336del	GRCh37
NC_000007.12:g.44155860_44155861del	NCBI36
NG_008847.1:g.44689_44690del
NG_008847.2:g.53436_53437del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*677+25_*677+26del	ENSP00000379142.4:n.*677+25_*677+26del
ENST00000616242.5:c.679+25_679+26del	ENSP00000482149.2:n.679+25_679+26del
ENST00000682635.1:n.1190_1191del
ENST00000345378.7:c.682+25_682+26del	ENSP00000223366.2:n.682+25_682+26del
ENST00000403799.8:c.679+25_679+26del MANE Select	ENSP00000384247.3:n.679+25_679+26del
ENST00000671824.1:c.679+25_679+26del	ENSP00000500264.1:n.679+25_679+26del
ENST00000673284.1:c.679+25_679+26del	ENSP00000499852.1:n.679+25_679+26del
ENST00000345378.6:c.682+25_682+26del	ENSP00000223366.2:n.682+25_682+26del
ENST00000395796.7:c.676+25_676+26del	ENSP00000379142.3:n.676+25_676+26del
ENST00000403799.7:c.679+25_679+26del	ENSP00000384247.3:n.679+25_679+26del
ENST00000437084.1:c.628+25_628+26del	ENSP00000402840.1:n.628+25_628+26del
ENST00000616242.4:c.676+25_676+26del	ENSP00000482149.1:n.676+25_676+26del
NM_000162.3:c.679+25_679+26del	NP_000153.1:n.679+25_679+26del
NM_033507.1:c.682+25_682+26del	NP_277042.1:n.682+25_682+26del
NM_033508.1:c.676+25_676+26del	NP_277043.1:n.676+25_676+26del
XR_927223.1:n.251_252del
NM_000162.4:c.679+25_679+26del	NP_000153.1:n.679+25_679+26del
NM_001354800.1:c.679+25_679+26del	NP_001341729.1:n.679+25_679+26del
NM_033507.2:c.682+25_682+26del	NP_277042.1:n.682+25_682+26del
NM_033508.2:c.676+25_676+26del	NP_277043.1:n.676+25_676+26del
XR_927223.2:n.251_252del
NM_000162.5:c.679+25_679+26del MANE Select	NP_000153.1:n.679+25_679+26del
NM_033507.3:c.682+25_682+26del	NP_277042.1:n.682+25_682+26del
NM_033508.3:c.676+25_676+26del	NP_277043.1:n.676+25_676+26del