Canonical Allele Identifier: CA2695203043

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145641_44145661del , CM000669.2:g.44145641_44145661del	GRCh38
NC_000007.13:g.44185240_44185260del , CM000669.1:g.44185240_44185260del	GRCh37
NC_000007.12:g.44151765_44151785del	NCBI36
NG_008847.1:g.48769_48789del
NG_008847.2:g.57516_57536del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1093_*1113del	ENSP00000379142.4:n.*1093_*1113del
ENST00000616242.5:c.*215_*235del	ENSP00000482149.2:n.*215_*235del
ENST00000683378.1:n.321_341del
ENST00000336642.9:c.129_149del	ENSP00000338009.5:p.Asp43_Cys49del
ENST00000345378.7:c.1098_1118del	ENSP00000223366.2:p.Asp366_Cys372del
ENST00000403799.8:c.1095_1115del MANE Select	ENSP00000384247.3:p.Asp365_Cys371del
ENST00000671824.1:c.1158_1178del	ENSP00000500264.1:p.Asp386_Cys392del
ENST00000672743.1:n.107_127del
ENST00000673284.1:c.1095_1115del	ENSP00000499852.1:p.Asp365_Cys371del
ENST00000336642.8:c.147_167del	ENSP00000338009.4:p.Asp49_Cys55del
ENST00000345378.6:c.1098_1118del	ENSP00000223366.2:p.Asp366_Cys372del
ENST00000395796.7:c.1092_1112del	ENSP00000379142.3:p.Asp364_Cys370del
ENST00000403799.7:c.1095_1115del	ENSP00000384247.3:p.Asp365_Cys371del
ENST00000437084.1:c.1044_1064del	ENSP00000402840.1:p.Asp348_Cys354del
ENST00000459642.1:n.475_495del
ENST00000616242.4:c.1092_1112del	ENSP00000482149.1:p.Asp364_Cys370del
NM_000162.3:c.1095_1115del	NP_000153.1:p.Asp365_Cys371del
NM_033507.1:c.1098_1118del	NP_277042.1:p.Asp366_Cys372del
NM_033508.1:c.1092_1112del	NP_277043.1:p.Asp364_Cys370del
NM_000162.4:c.1095_1115del	NP_000153.1:p.Asp365_Cys371del
NM_001354800.1:c.1095_1115del	NP_001341729.1:p.Asp365_Cys371del
NM_001354801.1:c.84_104del	NP_001341730.1:p.Asp28_Cys34del
NM_001354802.1:c.-46_-26del	NP_001341731.1:n.-46_-26del
NM_001354803.1:c.129_149del	NP_001341732.1:p.Asp43_Cys49del
NM_033507.2:c.1098_1118del	NP_277042.1:p.Asp366_Cys372del
NM_033508.2:c.1092_1112del	NP_277043.1:p.Asp364_Cys370del
XM_024446707.1:c.-46_-26del	XP_024302475.1:n.-46_-26del
NM_000162.5:c.1095_1115del MANE Select	NP_000153.1:p.Asp365_Cys371del
NM_033507.3:c.1098_1118del	NP_277042.1:p.Asp366_Cys372del
NM_033508.3:c.1092_1112del	NP_277043.1:p.Asp364_Cys370del
NM_001354803.2:c.129_149del	NP_001341732.1:p.Asp43_Cys49del