Canonical Allele Identifier: CA2682585903

Gene: GCK

Linked Data

• gnomAD v4: 7-44146457-GCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146461_44146462del , CM000669.2:g.44146461_44146462del	GRCh38
NC_000007.13:g.44186060_44186061del , CM000669.1:g.44186060_44186061del	GRCh37
NC_000007.12:g.44152585_44152586del	NCBI36
NG_008847.1:g.47965_47966del
NG_008847.2:g.56712_56713del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1017+4_*1017+5del	ENSP00000379142.4:n.*1017+4_*1017+5del
ENST00000616242.5:c.*139+4_*139+5del	ENSP00000482149.2:n.*139+4_*139+5del
ENST00000683378.1:n.245+4_245+5del
ENST00000345378.7:c.1022+4_1022+5del	ENSP00000223366.2:n.1022+4_1022+5del
ENST00000403799.8:c.1019+4_1019+5del MANE Select	ENSP00000384247.3:n.1019+4_1019+5del
ENST00000671824.1:c.1082+4_1082+5del	ENSP00000500264.1:n.1082+4_1082+5del
ENST00000673284.1:c.1019+4_1019+5del	ENSP00000499852.1:n.1019+4_1019+5del
ENST00000345378.6:c.1022+4_1022+5del	ENSP00000223366.2:n.1022+4_1022+5del
ENST00000395796.7:c.1016+4_1016+5del	ENSP00000379142.3:n.1016+4_1016+5del
ENST00000403799.7:c.1019+4_1019+5del	ENSP00000384247.3:n.1019+4_1019+5del
ENST00000437084.1:c.968+4_968+5del	ENSP00000402840.1:n.968+4_968+5del
ENST00000473353.1:n.317+4_317+5del
ENST00000616242.4:c.1016+4_1016+5del	ENSP00000482149.1:n.1016+4_1016+5del
NM_000162.3:c.1019+4_1019+5del	NP_000153.1:n.1019+4_1019+5del
NM_033507.1:c.1022+4_1022+5del	NP_277042.1:n.1022+4_1022+5del
NM_033508.1:c.1016+4_1016+5del	NP_277043.1:n.1016+4_1016+5del
NM_000162.4:c.1019+4_1019+5del	NP_000153.1:n.1019+4_1019+5del
NM_001354800.1:c.1019+4_1019+5del	NP_001341729.1:n.1019+4_1019+5del
NM_001354801.1:c.8+160_8+161del	NP_001341730.1:n.8+160_8+161del
NM_033507.2:c.1022+4_1022+5del	NP_277042.1:n.1022+4_1022+5del
NM_033508.2:c.1016+4_1016+5del	NP_277043.1:n.1016+4_1016+5del
NM_000162.5:c.1019+4_1019+5del MANE Select	NP_000153.1:n.1019+4_1019+5del
NM_033507.3:c.1022+4_1022+5del	NP_277042.1:n.1022+4_1022+5del
NM_033508.3:c.1016+4_1016+5del	NP_277043.1:n.1016+4_1016+5del