Canonical Allele Identifier: CA1703613051
Gene: GCK HGNC NCBI

Linked Data

dbSNP Id: rs2096272231
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145846_44145847insGA , CM000669.2:g.44145846_44145847insGA GRCh38
NC_000007.13:g.44185445_44185446insGA , CM000669.1:g.44185445_44185446insGA GRCh37
NC_000007.12:g.44151970_44151971insGA NCBI36
NG_008847.1:g.48577_48578insTC
NG_008847.2:g.57324_57325insTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1018-117_*1018-116insTC ENSP00000379142.4:n.*1018-117_*1018-116insTC
ENST00000616242.5:c.*140-117_*140-116insTC ENSP00000482149.2:n.*140-117_*140-116insTC
ENST00000683378.1:n.246-117_246-116insTC
ENST00000336642.9:c.54-117_54-116insTC ENSP00000338009.5:n.54-117_54-116insTC
ENST00000345378.7:c.1023-117_1023-116insTC ENSP00000223366.2:n.1023-117_1023-116insTC
ENST00000403799.8:c.1020-117_1020-116insTC MANE Select ENSP00000384247.3:n.1020-117_1020-116insTC
ENST00000671824.1:c.1083-117_1083-116insTC ENSP00000500264.1:n.1083-117_1083-116insTC
ENST00000672743.1:n.31+62_31+63insTC
ENST00000673284.1:c.1020-117_1020-116insTC ENSP00000499852.1:n.1020-117_1020-116insTC
ENST00000336642.8:c.72-117_72-116insTC ENSP00000338009.4:n.72-117_72-116insTC
ENST00000345378.6:c.1023-117_1023-116insTC ENSP00000223366.2:n.1023-117_1023-116insTC
ENST00000395796.7:c.1017-117_1017-116insTC ENSP00000379142.3:n.1017-117_1017-116insTC
ENST00000403799.7:c.1020-117_1020-116insTC ENSP00000384247.3:n.1020-117_1020-116insTC
ENST00000437084.1:c.969-117_969-116insTC ENSP00000402840.1:n.969-117_969-116insTC
ENST00000459642.1:n.283_284insTC
ENST00000473353.1:n.318-117_318-116insTC
ENST00000616242.4:c.1017-117_1017-116insTC ENSP00000482149.1:n.1017-117_1017-116insTC
NM_000162.3:c.1020-117_1020-116insTC NP_000153.1:n.1020-117_1020-116insTC
NM_033507.1:c.1023-117_1023-116insTC NP_277042.1:n.1023-117_1023-116insTC
NM_033508.1:c.1017-117_1017-116insTC NP_277043.1:n.1017-117_1017-116insTC
NM_000162.4:c.1020-117_1020-116insTC NP_000153.1:n.1020-117_1020-116insTC
NM_001354800.1:c.1020-117_1020-116insTC NP_001341729.1:n.1020-117_1020-116insTC
NM_001354801.1:c.9-117_9-116insTC NP_001341730.1:n.9-117_9-116insTC
NM_001354802.1:c.-122+62_-122+63insTC NP_001341731.1:n.-122+62_-122+63insTC
NM_001354803.1:c.54-117_54-116insTC NP_001341732.1:n.54-117_54-116insTC
NM_033507.2:c.1023-117_1023-116insTC NP_277042.1:n.1023-117_1023-116insTC
NM_033508.2:c.1017-117_1017-116insTC NP_277043.1:n.1017-117_1017-116insTC
XM_024446707.1:c.-122+62_-122+63insTC XP_024302475.1:n.-122+62_-122+63insTC
NM_000162.5:c.1020-117_1020-116insTC MANE Select NP_000153.1:n.1020-117_1020-116insTC
NM_033507.3:c.1023-117_1023-116insTC NP_277042.1:n.1023-117_1023-116insTC
NM_033508.3:c.1017-117_1017-116insTC NP_277043.1:n.1017-117_1017-116insTC
NM_001354803.2:c.54-117_54-116insTC NP_001341732.1:n.54-117_54-116insTC
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