Canonical Allele Identifier: CA1703613015
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145797C= , CM000669.2:g.44145797C= GRCh38
NC_000007.13:g.44185396C= , CM000669.1:g.44185396C= GRCh37
NC_000007.12:g.44151921C= NCBI36
NG_008847.1:g.48627G=
NG_008847.2:g.57374G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1018-67G= ENSP00000379142.4:n.*1018-67G=
ENST00000616242.5:c.*140-67G= ENSP00000482149.2:n.*140-67G=
ENST00000683378.1:n.246-67G=
ENST00000336642.9:c.54-67G= ENSP00000338009.5:n.54-67G=
ENST00000345378.7:c.1023-67G= ENSP00000223366.2:n.1023-67G=
ENST00000403799.8:c.1020-67G= MANE Select ENSP00000384247.3:n.1020-67G=
ENST00000671824.1:c.1083-67G= ENSP00000500264.1:n.1083-67G=
ENST00000672743.1:n.32-67G=
ENST00000673284.1:c.1020-67G= ENSP00000499852.1:n.1020-67G=
ENST00000336642.8:c.72-67G= ENSP00000338009.4:n.72-67G=
ENST00000345378.6:c.1023-67G= ENSP00000223366.2:n.1023-67G=
ENST00000395796.7:c.1017-67G= ENSP00000379142.3:n.1017-67G=
ENST00000403799.7:c.1020-67G= ENSP00000384247.3:n.1020-67G=
ENST00000437084.1:c.969-67G= ENSP00000402840.1:n.969-67G=
ENST00000459642.1:n.333G=
ENST00000473353.1:n.318-67G=
ENST00000616242.4:c.1017-67G= ENSP00000482149.1:n.1017-67G=
NM_000162.3:c.1020-67G= NP_000153.1:n.1020-67G=
NM_033507.1:c.1023-67G= NP_277042.1:n.1023-67G=
NM_033508.1:c.1017-67G= NP_277043.1:n.1017-67G=
NM_000162.4:c.1020-67G= NP_000153.1:n.1020-67G=
NM_001354800.1:c.1020-67G= NP_001341729.1:n.1020-67G=
NM_001354801.1:c.9-67G= NP_001341730.1:n.9-67G=
NM_001354802.1:c.-121-67G= NP_001341731.1:n.-121-67G=
NM_001354803.1:c.54-67G= NP_001341732.1:n.54-67G=
NM_033507.2:c.1023-67G= NP_277042.1:n.1023-67G=
NM_033508.2:c.1017-67G= NP_277043.1:n.1017-67G=
XM_024446707.1:c.-121-67G= XP_024302475.1:n.-121-67G=
NM_000162.5:c.1020-67G= MANE Select NP_000153.1:n.1020-67G=
NM_033507.3:c.1023-67G= NP_277042.1:n.1023-67G=
NM_033508.3:c.1017-67G= NP_277043.1:n.1017-67G=
NM_001354803.2:c.54-67G= NP_001341732.1:n.54-67G=