Canonical Allele Identifier: CA2682584884

Gene: GCK

Linked Data

• gnomAD v4: 7-44146273-GGGCCCCGCCCACTCCCCCGCCCCCTGTGCCCCGCCCCGGGCCCCGCCCACGCCCGGAATCCCGCCCCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146279_44146346del , CM000669.2:g.44146279_44146346del	GRCh38
NC_000007.13:g.44185878_44185945del , CM000669.1:g.44185878_44185945del	GRCh37
NC_000007.12:g.44152403_44152470del	NCBI36
NG_008847.1:g.48083_48150del
NG_008847.2:g.56830_56897del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1017+122_*1017+189del	ENSP00000379142.4:n.*1017+122_*1017+189del
ENST00000616242.5:c.*139+122_*139+189del	ENSP00000482149.2:n.*139+122_*139+189del
ENST00000683378.1:n.245+122_245+189del
ENST00000345378.7:c.1022+122_1022+189del	ENSP00000223366.2:n.1022+122_1022+189del
ENST00000403799.8:c.1019+122_1019+189del MANE Select	ENSP00000384247.3:n.1019+122_1019+189del
ENST00000671824.1:c.1082+122_1082+189del	ENSP00000500264.1:n.1082+122_1082+189del
ENST00000673284.1:c.1019+122_1019+189del	ENSP00000499852.1:n.1019+122_1019+189del
ENST00000345378.6:c.1022+122_1022+189del	ENSP00000223366.2:n.1022+122_1022+189del
ENST00000395796.7:c.1016+122_1016+189del	ENSP00000379142.3:n.1016+122_1016+189del
ENST00000403799.7:c.1019+122_1019+189del	ENSP00000384247.3:n.1019+122_1019+189del
ENST00000437084.1:c.968+122_968+189del	ENSP00000402840.1:n.968+122_968+189del
ENST00000473353.1:n.317+122_317+189del
ENST00000616242.4:c.1016+122_1016+189del	ENSP00000482149.1:n.1016+122_1016+189del
NM_000162.3:c.1019+122_1019+189del	NP_000153.1:n.1019+122_1019+189del
NM_033507.1:c.1022+122_1022+189del	NP_277042.1:n.1022+122_1022+189del
NM_033508.1:c.1016+122_1016+189del	NP_277043.1:n.1016+122_1016+189del
NM_000162.4:c.1019+122_1019+189del	NP_000153.1:n.1019+122_1019+189del
NM_001354800.1:c.1019+122_1019+189del	NP_001341729.1:n.1019+122_1019+189del
NM_001354801.1:c.8+278_8+345del	NP_001341730.1:n.8+278_8+345del
NM_033507.2:c.1022+122_1022+189del	NP_277042.1:n.1022+122_1022+189del
NM_033508.2:c.1016+122_1016+189del	NP_277043.1:n.1016+122_1016+189del
NM_000162.5:c.1019+122_1019+189del MANE Select	NP_000153.1:n.1019+122_1019+189del
NM_033507.3:c.1022+122_1022+189del	NP_277042.1:n.1022+122_1022+189del
NM_033508.3:c.1016+122_1016+189del	NP_277043.1:n.1016+122_1016+189del