Canonical Allele Identifier: CA367398767
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447383
dbSNP Id: rs193922266

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145608A>T , CM000669.2:g.44145608A>T GRCh38
NC_000007.13:g.44185207A>T , CM000669.1:g.44185207A>T GRCh37
NC_000007.12:g.44151732A>T NCBI36
NG_008847.1:g.48816T>A
NG_008847.2:g.57563T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1140T>A ENSP00000379142.4:n.*1140T>A
ENST00000616242.5:c.*262T>A ENSP00000482149.2:n.*262T>A
ENST00000683378.1:n.368T>A
ENST00000336642.9:c.176T>A ENSP00000338009.5:p.Met59Lys
ENST00000345378.7:c.1145T>A ENSP00000223366.2:p.Met382Lys
ENST00000403799.8:c.1142T>A MANE Select ENSP00000384247.3:p.Met381Lys
ENST00000671824.1:c.1205T>A ENSP00000500264.1:p.Met402Lys
ENST00000672743.1:n.154T>A
ENST00000673284.1:c.1142T>A ENSP00000499852.1:p.Met381Lys
ENST00000336642.8:c.194T>A ENSP00000338009.4:p.Met65Lys
ENST00000345378.6:c.1145T>A ENSP00000223366.2:p.Met382Lys
ENST00000395796.7:c.1139T>A ENSP00000379142.3:p.Met380Lys
ENST00000403799.7:c.1142T>A ENSP00000384247.3:p.Met381Lys
ENST00000437084.1:c.1091T>A ENSP00000402840.1:p.Met364Lys
ENST00000459642.1:n.522T>A
ENST00000616242.4:c.1139T>A ENSP00000482149.1:p.Met380Lys
NM_000162.3:c.1142T>A NP_000153.1:p.Met381Lys
NM_033507.1:c.1145T>A NP_277042.1:p.Met382Lys
NM_033508.1:c.1139T>A NP_277043.1:p.Met380Lys
NM_000162.4:c.1142T>A NP_000153.1:p.Met381Lys
NM_001354800.1:c.1142T>A NP_001341729.1:p.Met381Lys
NM_001354801.1:c.131T>A NP_001341730.1:p.Met44Lys
NM_001354802.1:c.2T>A NP_001341731.1:p.Met1Lys
NM_001354803.1:c.176T>A NP_001341732.1:p.Met59Lys
NM_033507.2:c.1145T>A NP_277042.1:p.Met382Lys
NM_033508.2:c.1139T>A NP_277043.1:p.Met380Lys
XM_024446707.1:c.2T>A XP_024302475.1:p.Met1Lys
NM_000162.5:c.1142T>A MANE Select NP_000153.1:p.Met381Lys
NM_033507.3:c.1145T>A NP_277042.1:p.Met382Lys
NM_033508.3:c.1139T>A NP_277043.1:p.Met380Lys
NM_001354803.2:c.176T>A NP_001341732.1:p.Met59Lys