Canonical Allele Identifier: CA2682579129
Gene: GCK HGNC NCBI

Linked Data

gnomAD v4: 7-44144879-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44144879C>A , CM000669.2:g.44144879C>A GRCh38
NC_000007.13:g.44184478C>A , CM000669.1:g.44184478C>A GRCh37
NC_000007.12:g.44151003C>A NCBI36
NG_008847.1:g.49545G>T
NG_008847.2:g.58292G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1653G>T ENSP00000379142.4:n.*1653G>T
ENST00000616242.5:c.*775G>T ENSP00000482149.2:n.*775G>T
ENST00000683378.1:n.881G>T
ENST00000336642.9:c.*257G>T ENSP00000338009.5:n.*257G>T
ENST00000345378.7:c.*257G>T ENSP00000223366.2:n.*257G>T
ENST00000403799.8:c.*257G>T MANE Select ENSP00000384247.3:n.*257G>T
ENST00000671824.1:c.*257G>T ENSP00000500264.1:n.*257G>T
ENST00000672743.1:n.381+286G>T
ENST00000673284.1:c.1369+286G>T ENSP00000499852.1:n.1369+286G>T
ENST00000336642.8:c.707G>T ENSP00000338009.4:n.707G>T
ENST00000345378.6:c.*257G>T ENSP00000223366.2:n.*257G>T
ENST00000395796.7:c.*257G>T ENSP00000379142.3:n.*257G>T
ENST00000403799.7:c.*257G>T ENSP00000384247.3:n.*257G>T
ENST00000459642.1:n.1035G>T
ENST00000616242.4:c.1652G>T ENSP00000482149.1:n.1652G>T
NM_000162.3:c.*257G>T NP_000153.1:n.*257G>T
NM_033507.1:c.*257G>T NP_277042.1:n.*257G>T
NM_033508.1:c.*257G>T NP_277043.1:n.*257G>T
NM_000162.4:c.*257G>T NP_000153.1:n.*257G>T
NM_001354800.1:c.1369+286G>T NP_001341729.1:n.1369+286G>T
NM_001354801.1:c.*257G>T NP_001341730.1:n.*257G>T
NM_001354802.1:c.229+286G>T NP_001341731.1:n.229+286G>T
NM_001354803.1:c.*257G>T NP_001341732.1:n.*257G>T
NM_033507.2:c.*257G>T NP_277042.1:n.*257G>T
NM_033508.2:c.*257G>T NP_277043.1:n.*257G>T
XM_024446707.1:c.*257G>T XP_024302475.1:n.*257G>T
NM_000162.5:c.*257G>T MANE Select NP_000153.1:n.*257G>T
NM_033507.3:c.*257G>T NP_277042.1:n.*257G>T
NM_033508.3:c.*257G>T NP_277043.1:n.*257G>T
NM_001354803.2:c.*257G>T NP_001341732.1:n.*257G>T