Canonical Allele Identifier: CA2695203058

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146463del , CM000669.2:g.44146463del	GRCh38
NC_000007.13:g.44186062del , CM000669.1:g.44186062del	GRCh37
NC_000007.12:g.44152587del	NCBI36
NG_008847.1:g.47962del
NG_008847.2:g.56709del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1017+1del
ENST00000616242.5:c.*139+1del
ENST00000683378.1:n.245+1del
ENST00000345378.7:c.1022+1del
ENST00000403799.8:c.1019+1del
ENST00000671824.1:c.1082+1del
ENST00000673284.1:c.1019+1del
ENST00000345378.6:c.1022+1del
ENST00000395796.7:c.1016+1del
ENST00000403799.7:c.1019+1del
ENST00000437084.1:c.968+1del
ENST00000473353.1:n.317+1del
ENST00000616242.4:c.1016+1del
NM_000162.3:c.1019+1del
NM_033507.1:c.1022+1del
NM_033508.1:c.1016+1del
NM_000162.4:c.1019+1del
NM_001354800.1:c.1019+1del
NM_001354801.1:c.8+157del	NP_001341730.1:n.8+157del
NM_033507.2:c.1022+1del
NM_033508.2:c.1016+1del
NM_000162.5:c.1019+1del
NM_033507.3:c.1022+1del
NM_033508.3:c.1016+1del