Canonical Allele Identifier: CA2695202992

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145559_44145566del , CM000669.2:g.44145559_44145566del	GRCh38
NC_000007.13:g.44185158_44185165del , CM000669.1:g.44185158_44185165del	GRCh37
NC_000007.12:g.44151683_44151690del	NCBI36
NG_008847.1:g.48860_48867del
NG_008847.2:g.57607_57614del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1184_*1191del	ENSP00000379142.4:n.*1184_*1191del
ENST00000616242.5:c.*306_*313del	ENSP00000482149.2:n.*306_*313del
ENST00000683378.1:n.412_419del
ENST00000336642.9:c.220_227del	ENSP00000338009.5:p.Ser74ArgfsTer?
ENST00000345378.7:c.1189_1196del	ENSP00000223366.2:p.Ser397ArgfsTer?
ENST00000403799.8:c.1186_1193del MANE Select	ENSP00000384247.3:p.Ser396ArgfsTer?
ENST00000671824.1:c.1249_1256del	ENSP00000500264.1:p.Ser417ArgfsTer?
ENST00000672743.1:n.198_205del
ENST00000673284.1:c.1186_1193del	ENSP00000499852.1:p.Ser396ArgfsTer?
ENST00000336642.8:c.238_245del	ENSP00000338009.4:p.Ser80ArgfsTer?
ENST00000345378.6:c.1189_1196del	ENSP00000223366.2:p.Ser397ArgfsTer?
ENST00000395796.7:c.1183_1190del	ENSP00000379142.3:p.Ser395ArgfsTer?
ENST00000403799.7:c.1186_1193del	ENSP00000384247.3:p.Ser396ArgfsTer?
ENST00000437084.1:c.1135_1142del	ENSP00000402840.1:p.Ser379ArgfsTer?
ENST00000459642.1:n.566_573del
ENST00000616242.4:c.1183_1190del	ENSP00000482149.1:p.Ser395ArgfsTer?
NM_000162.3:c.1186_1193del	NP_000153.1:p.Ser396ArgfsTer?
NM_033507.1:c.1189_1196del	NP_277042.1:p.Ser397ArgfsTer?
NM_033508.1:c.1183_1190del	NP_277043.1:p.Ser395ArgfsTer?
NM_000162.4:c.1186_1193del	NP_000153.1:p.Ser396ArgfsTer?
NM_001354800.1:c.1186_1193del	NP_001341729.1:p.Ser396ArgfsTer?
NM_001354801.1:c.175_182del	NP_001341730.1:p.Ser59ArgfsTer?
NM_001354802.1:c.46_53del	NP_001341731.1:p.Ser16ArgfsTer?
NM_001354803.1:c.220_227del	NP_001341732.1:p.Ser74ArgfsTer?
NM_033507.2:c.1189_1196del	NP_277042.1:p.Ser397ArgfsTer?
NM_033508.2:c.1183_1190del	NP_277043.1:p.Ser395ArgfsTer?
XM_024446707.1:c.46_53del	XP_024302475.1:p.Ser16ArgfsTer?
NM_000162.5:c.1186_1193del MANE Select	NP_000153.1:p.Ser396ArgfsTer?
NM_033507.3:c.1189_1196del	NP_277042.1:p.Ser397ArgfsTer?
NM_033508.3:c.1183_1190del	NP_277043.1:p.Ser395ArgfsTer?
NM_001354803.2:c.220_227del	NP_001341732.1:p.Ser74ArgfsTer?