Canonical Allele Identifier: CA2695202963

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145251_44145259del , CM000669.2:g.44145251_44145259del	GRCh38
NC_000007.13:g.44184850_44184858del , CM000669.1:g.44184850_44184858del	GRCh37
NC_000007.12:g.44151375_44151383del	NCBI36
NG_008847.1:g.49168_49176del
NG_008847.2:g.57915_57923del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1276_*1284del	ENSP00000379142.4:n.*1276_*1284del
ENST00000616242.5:c.*398_*406del	ENSP00000482149.2:n.*398_*406del
ENST00000683378.1:n.504_512del
ENST00000336642.9:c.312_320del	ENSP00000338009.5:p.Ser104_Arg106del
ENST00000345378.7:c.1281_1289del	ENSP00000223366.2:p.Ser427_Arg429del
ENST00000403799.8:c.1278_1286del MANE Select	ENSP00000384247.3:p.Ser426_Arg428del
ENST00000671824.1:c.1341_1349del	ENSP00000500264.1:p.Ser447_Arg449del
ENST00000672743.1:n.290_298del
ENST00000673284.1:c.1278_1286del	ENSP00000499852.1:p.Ser426_Arg428del
ENST00000336642.8:c.330_338del	ENSP00000338009.4:p.Ser110_Arg112del
ENST00000345378.6:c.1281_1289del	ENSP00000223366.2:p.Ser427_Arg429del
ENST00000395796.7:c.1275_1283del	ENSP00000379142.3:p.Ser425_Arg427del
ENST00000403799.7:c.1278_1286del	ENSP00000384247.3:p.Ser426_Arg428del
ENST00000437084.1:c.1227_1235del	ENSP00000402840.1:p.Ser409_Arg411del
ENST00000459642.1:n.658_666del
ENST00000616242.4:c.1275_1283del	ENSP00000482149.1:p.Ser425_Arg427del
NM_000162.3:c.1278_1286del	NP_000153.1:p.Ser426_Arg428del
NM_033507.1:c.1281_1289del	NP_277042.1:p.Ser427_Arg429del
NM_033508.1:c.1275_1283del	NP_277043.1:p.Ser425_Arg427del
NM_000162.4:c.1278_1286del	NP_000153.1:p.Ser426_Arg428del
NM_001354800.1:c.1278_1286del	NP_001341729.1:p.Ser426_Arg428del
NM_001354801.1:c.267_275del	NP_001341730.1:p.Ser89_Arg91del
NM_001354802.1:c.138_146del	NP_001341731.1:p.Ser46_Arg48del
NM_001354803.1:c.312_320del	NP_001341732.1:p.Ser104_Arg106del
NM_033507.2:c.1281_1289del	NP_277042.1:p.Ser427_Arg429del
NM_033508.2:c.1275_1283del	NP_277043.1:p.Ser425_Arg427del
XM_024446707.1:c.138_146del	XP_024302475.1:p.Ser46_Arg48del
NM_000162.5:c.1278_1286del MANE Select	NP_000153.1:p.Ser426_Arg428del
NM_033507.3:c.1281_1289del	NP_277042.1:p.Ser427_Arg429del
NM_033508.3:c.1275_1283del	NP_277043.1:p.Ser425_Arg427del
NM_001354803.2:c.312_320del	NP_001341732.1:p.Ser104_Arg106del