Canonical Allele Identifier: CA3004402170

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44149744_44149745del , CM000669.2:g.44149744_44149745del	GRCh38
NC_000007.13:g.44189343_44189344del , CM000669.1:g.44189343_44189344del	GRCh37
NC_000007.12:g.44155868_44155869del	NCBI36
NG_008847.1:g.44680_44681del
NG_008847.2:g.53427_53428del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*677+16_*677+17del	ENSP00000379142.4:n.*677+16_*677+17del
ENST00000616242.5:c.679+16_679+17del	ENSP00000482149.2:n.679+16_679+17del
ENST00000682635.1:n.1181_1182del
ENST00000345378.7:c.682+16_682+17del	ENSP00000223366.2:n.682+16_682+17del
ENST00000403799.8:c.679+16_679+17del MANE Select	ENSP00000384247.3:n.679+16_679+17del
ENST00000671824.1:c.679+16_679+17del	ENSP00000500264.1:n.679+16_679+17del
ENST00000673284.1:c.679+16_679+17del	ENSP00000499852.1:n.679+16_679+17del
ENST00000345378.6:c.682+16_682+17del	ENSP00000223366.2:n.682+16_682+17del
ENST00000395796.7:c.676+16_676+17del	ENSP00000379142.3:n.676+16_676+17del
ENST00000403799.7:c.679+16_679+17del	ENSP00000384247.3:n.679+16_679+17del
ENST00000437084.1:c.628+16_628+17del	ENSP00000402840.1:n.628+16_628+17del
ENST00000616242.4:c.676+16_676+17del	ENSP00000482149.1:n.676+16_676+17del
NM_000162.3:c.679+16_679+17del	NP_000153.1:n.679+16_679+17del
NM_033507.1:c.682+16_682+17del	NP_277042.1:n.682+16_682+17del
NM_033508.1:c.676+16_676+17del	NP_277043.1:n.676+16_676+17del
XR_927223.1:n.259_260del
NM_000162.4:c.679+16_679+17del	NP_000153.1:n.679+16_679+17del
NM_001354800.1:c.679+16_679+17del	NP_001341729.1:n.679+16_679+17del
NM_033507.2:c.682+16_682+17del	NP_277042.1:n.682+16_682+17del
NM_033508.2:c.676+16_676+17del	NP_277043.1:n.676+16_676+17del
XR_927223.2:n.259_260del
NM_000162.5:c.679+16_679+17del MANE Select	NP_000153.1:n.679+16_679+17del
NM_033507.3:c.682+16_682+17del	NP_277042.1:n.682+16_682+17del
NM_033508.3:c.676+16_676+17del	NP_277043.1:n.676+16_676+17del