Canonical Allele Identifier: CA2682584910

Gene: GCK

Linked Data

• gnomAD v4: 7-44146275-G-GGC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146275_44146276insGC , CM000669.2:g.44146275_44146276insGC	GRCh38
NC_000007.13:g.44185874_44185875insGC , CM000669.1:g.44185874_44185875insGC	GRCh37
NC_000007.12:g.44152399_44152400insGC	NCBI36
NG_008847.1:g.48148_48149insGC
NG_008847.2:g.56895_56896insGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1017+187_*1017+188insGC	ENSP00000379142.4:n.*1017+187_*1017+188insGC
ENST00000616242.5:c.*139+187_*139+188insGC	ENSP00000482149.2:n.*139+187_*139+188insGC
ENST00000683378.1:n.245+187_245+188insGC
ENST00000345378.7:c.1022+187_1022+188insGC	ENSP00000223366.2:n.1022+187_1022+188insGC
ENST00000403799.8:c.1019+187_1019+188insGC MANE Select	ENSP00000384247.3:n.1019+187_1019+188insGC
ENST00000671824.1:c.1082+187_1082+188insGC	ENSP00000500264.1:n.1082+187_1082+188insGC
ENST00000673284.1:c.1019+187_1019+188insGC	ENSP00000499852.1:n.1019+187_1019+188insGC
ENST00000345378.6:c.1022+187_1022+188insGC	ENSP00000223366.2:n.1022+187_1022+188insGC
ENST00000395796.7:c.1016+187_1016+188insGC	ENSP00000379142.3:n.1016+187_1016+188insGC
ENST00000403799.7:c.1019+187_1019+188insGC	ENSP00000384247.3:n.1019+187_1019+188insGC
ENST00000437084.1:c.968+187_968+188insGC	ENSP00000402840.1:n.968+187_968+188insGC
ENST00000473353.1:n.317+187_317+188insGC
ENST00000616242.4:c.1016+187_1016+188insGC	ENSP00000482149.1:n.1016+187_1016+188insGC
NM_000162.3:c.1019+187_1019+188insGC	NP_000153.1:n.1019+187_1019+188insGC
NM_033507.1:c.1022+187_1022+188insGC	NP_277042.1:n.1022+187_1022+188insGC
NM_033508.1:c.1016+187_1016+188insGC	NP_277043.1:n.1016+187_1016+188insGC
NM_000162.4:c.1019+187_1019+188insGC	NP_000153.1:n.1019+187_1019+188insGC
NM_001354800.1:c.1019+187_1019+188insGC	NP_001341729.1:n.1019+187_1019+188insGC
NM_001354801.1:c.8+343_8+344insGC	NP_001341730.1:n.8+343_8+344insGC
NM_033507.2:c.1022+187_1022+188insGC	NP_277042.1:n.1022+187_1022+188insGC
NM_033508.2:c.1016+187_1016+188insGC	NP_277043.1:n.1016+187_1016+188insGC
NM_000162.5:c.1019+187_1019+188insGC MANE Select	NP_000153.1:n.1019+187_1019+188insGC
NM_033507.3:c.1022+187_1022+188insGC	NP_277042.1:n.1022+187_1022+188insGC
NM_033508.3:c.1016+187_1016+188insGC	NP_277043.1:n.1016+187_1016+188insGC