Canonical Allele Identifier: CA1703612618

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145095_44145121delinsGTGGGGCTGTGGCATCCTCCCTGCGCT , CM000669.2:g.44145095_44145121delinsGTGGGGCTGTGGCATCCTCCCTGCGCT	GRCh38
NC_000007.13:g.44184694_44184720delinsGTGGGGCTGTGGCATCCTCCCTGCGCT , CM000669.1:g.44184694_44184720delinsGTGGGGCTGTGGCATCCTCCCTGCGCT	GRCh37
NC_000007.12:g.44151219_44151245delinsGTGGGGCTGTGGCATCCTCCCTGCGCT	NCBI36
NG_008847.1:g.49303_49329delinsAGCGCAGGGAGGATGCCACAGCCCCAC
NG_008847.2:g.58050_58076delinsAGCGCAGGGAGGATGCCACAGCCCCAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*1411_*1437delinsAGCGCAGGGAGGATGCCACAGCCCCAC	ENSP00000379142.4:n.*1411_*1437delinsAGCG...
ENST00000616242.5:c.*533_*559delinsAGCGCAGGGAGGATGCCACAGCCCCAC	ENSP00000482149.2:n.*533_*559delinsAGCGCA...
ENST00000683378.1:n.639_665delinsAGCGCAGGGAGGATGCCACAGCCCCAC
ENST00000336642.9:c.*15_*41delinsAGCGCAGGGAGGATGCCACAGCCCCAC	ENSP00000338009.5:n.*15_*41delinsAGCGCAGG...
ENST00000345378.7:c.*15_*41delinsAGCGCAGGGAGGATGCCACAGCCCCAC	ENSP00000223366.2:n.*15_*41delinsAGCGCAGG...
ENST00000403799.8:c.*15_*41delinsAGCGCAGGGAGGATGCCACAGCCCCAC MANE Select	ENSP00000384247.3:n.*15_*41delinsAGCGCAGG...
ENST00000671824.1:c.*15_*41delinsAGCGCAGGGAGGATGCCACAGCCCCAC	ENSP00000500264.1:n.*15_*41delinsAGCGCAGG...
ENST00000672743.1:n.381+44_381+70delinsAGCGCAGGGAGGATGCCACAGCCCCAC
ENST00000673284.1:c.1369+44_1369+70delinsAGCGCAGGGAGGATGCCACAGCCCCAC	ENSP00000499852.1:n.1369+44_1369+70delins...
ENST00000336642.8:c.465_491delinsAGCGCAGGGAGGATGCCACAGCCCCAC	ENSP00000338009.4:n.465_491delinsAGCGCAGG...
ENST00000345378.6:c.*15_*41delinsAGCGCAGGGAGGATGCCACAGCCCCAC	ENSP00000223366.2:n.*15_*41delinsAGCGCAGG...
ENST00000395796.7:c.*15_*41delinsAGCGCAGGGAGGATGCCACAGCCCCAC	ENSP00000379142.3:n.*15_*41delinsAGCGCAGG...
ENST00000403799.7:c.*15_*41delinsAGCGCAGGGAGGATGCCACAGCCCCAC	ENSP00000384247.3:n.*15_*41delinsAGCGCAGG...
ENST00000459642.1:n.793_819delinsAGCGCAGGGAGGATGCCACAGCCCCAC
ENST00000616242.4:c.1410_1436delinsAGCGCAGGGAGGATGCCACAGCCCCAC	ENSP00000482149.1:n.1410_1436delinsAGCGCA...
NM_000162.3:c.*15_*41delinsAGCGCAGGGAGGATGCCACAGCCCCAC	NP_000153.1:n.*15_*41delinsAGCGCAGGGAGGAT...
NM_033507.1:c.*15_*41delinsAGCGCAGGGAGGATGCCACAGCCCCAC	NP_277042.1:n.*15_*41delinsAGCGCAGGGAGGAT...
NM_033508.1:c.*15_*41delinsAGCGCAGGGAGGATGCCACAGCCCCAC	NP_277043.1:n.*15_*41delinsAGCGCAGGGAGGAT...
NM_000162.4:c.*15_*41delinsAGCGCAGGGAGGATGCCACAGCCCCAC	NP_000153.1:n.*15_*41delinsAGCGCAGGGAGGAT...
NM_001354800.1:c.1369+44_1369+70delinsAGCGCAGGGAGGATGCCACAGCCCCAC	NP_001341729.1:n.1369+44_1369+70delinsAGC...
NM_001354801.1:c.*15_*41delinsAGCGCAGGGAGGATGCCACAGCCCCAC	NP_001341730.1:n.*15_*41delinsAGCGCAGGGAG...
NM_001354802.1:c.229+44_229+70delinsAGCGCAGGGAGGATGCCACAGCCCCAC	NP_001341731.1:n.229+44_229+70delinsAGCGC...
NM_001354803.1:c.*15_*41delinsAGCGCAGGGAGGATGCCACAGCCCCAC	NP_001341732.1:n.*15_*41delinsAGCGCAGGGAG...
NM_033507.2:c.*15_*41delinsAGCGCAGGGAGGATGCCACAGCCCCAC	NP_277042.1:n.*15_*41delinsAGCGCAGGGAGGAT...
NM_033508.2:c.*15_*41delinsAGCGCAGGGAGGATGCCACAGCCCCAC	NP_277043.1:n.*15_*41delinsAGCGCAGGGAGGAT...
XM_024446707.1:c.*15_*41delinsAGCGCAGGGAGGATGCCACAGCCCCAC	XP_024302475.1:n.*15_*41delinsAGCGCAGGGAG...
NM_000162.5:c.*15_*41delinsAGCGCAGGGAGGATGCCACAGCCCCAC MANE Select	NP_000153.1:n.*15_*41delinsAGCGCAGGGAGGAT...
NM_033507.3:c.*15_*41delinsAGCGCAGGGAGGATGCCACAGCCCCAC	NP_277042.1:n.*15_*41delinsAGCGCAGGGAGGAT...
NM_033508.3:c.*15_*41delinsAGCGCAGGGAGGATGCCACAGCCCCAC	NP_277043.1:n.*15_*41delinsAGCGCAGGGAGGAT...
NM_001354803.2:c.*15_*41delinsAGCGCAGGGAGGATGCCACAGCCCCAC	NP_001341732.1:n.*15_*41delinsAGCGCAGGGAG...