Canonical Allele Identifier: CA2695202987

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145543_44145544del , CM000669.2:g.44145543_44145544del	GRCh38
NC_000007.13:g.44185142_44185143del , CM000669.1:g.44185142_44185143del	GRCh37
NC_000007.12:g.44151667_44151668del	NCBI36
NG_008847.1:g.48882_48883del
NG_008847.2:g.57629_57630del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1206_*1207del	ENSP00000379142.4:n.*1206_*1207del
ENST00000616242.5:c.*328_*329del	ENSP00000482149.2:n.*328_*329del
ENST00000683378.1:n.434_435del
ENST00000336642.9:c.242_243del	ENSP00000338009.5:p.Arg81HisfsTer?
ENST00000345378.7:c.1211_1212del	ENSP00000223366.2:p.Arg404HisfsTer?
ENST00000403799.8:c.1208_1209del MANE Select	ENSP00000384247.3:p.Arg403HisfsTer?
ENST00000671824.1:c.1271_1272del	ENSP00000500264.1:p.Arg424HisfsTer?
ENST00000672743.1:n.220_221del
ENST00000673284.1:c.1208_1209del	ENSP00000499852.1:p.Arg403HisfsTer?
ENST00000336642.8:c.260_261del	ENSP00000338009.4:p.Arg87HisfsTer?
ENST00000345378.6:c.1211_1212del	ENSP00000223366.2:p.Arg404HisfsTer?
ENST00000395796.7:c.1205_1206del	ENSP00000379142.3:p.Arg402HisfsTer?
ENST00000403799.7:c.1208_1209del	ENSP00000384247.3:p.Arg403HisfsTer?
ENST00000437084.1:c.1157_1158del	ENSP00000402840.1:p.Arg386HisfsTer?
ENST00000459642.1:n.588_589del
ENST00000616242.4:c.1205_1206del	ENSP00000482149.1:p.Arg402HisfsTer?
NM_000162.3:c.1208_1209del	NP_000153.1:p.Arg403HisfsTer?
NM_033507.1:c.1211_1212del	NP_277042.1:p.Arg404HisfsTer?
NM_033508.1:c.1205_1206del	NP_277043.1:p.Arg402HisfsTer?
NM_000162.4:c.1208_1209del	NP_000153.1:p.Arg403HisfsTer?
NM_001354800.1:c.1208_1209del	NP_001341729.1:p.Arg403HisfsTer?
NM_001354801.1:c.197_198del	NP_001341730.1:p.Arg66HisfsTer?
NM_001354802.1:c.68_69del	NP_001341731.1:p.Arg23HisfsTer?
NM_001354803.1:c.242_243del	NP_001341732.1:p.Arg81HisfsTer?
NM_033507.2:c.1211_1212del	NP_277042.1:p.Arg404HisfsTer?
NM_033508.2:c.1205_1206del	NP_277043.1:p.Arg402HisfsTer?
XM_024446707.1:c.68_69del	XP_024302475.1:p.Arg23HisfsTer?
NM_000162.5:c.1208_1209del MANE Select	NP_000153.1:p.Arg403HisfsTer?
NM_033507.3:c.1211_1212del	NP_277042.1:p.Arg404HisfsTer?
NM_033508.3:c.1205_1206del	NP_277043.1:p.Arg402HisfsTer?
NM_001354803.2:c.242_243del	NP_001341732.1:p.Arg81HisfsTer?