Canonical Allele Identifier: CA1703612849
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145507G= , CM000669.2:g.44145507G= GRCh38
NC_000007.13:g.44185106G= , CM000669.1:g.44185106G= GRCh37
NC_000007.12:g.44151631G= NCBI36
NG_008847.1:g.48917C=
NG_008847.2:g.57664C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1241C= ENSP00000379142.4:n.*1241C=
ENST00000616242.5:c.*363C= ENSP00000482149.2:n.*363C=
ENST00000683378.1:n.469C=
ENST00000336642.9:c.277C= ENSP00000338009.5:p.Leu93=
ENST00000345378.7:c.1246C= ENSP00000223366.2:p.Leu416=
ENST00000403799.8:c.1243C= MANE Select ENSP00000384247.3:p.Leu415=
ENST00000671824.1:c.1306C= ENSP00000500264.1:p.Leu436=
ENST00000672743.1:n.255C=
ENST00000673284.1:c.1243C= ENSP00000499852.1:p.Leu415=
ENST00000336642.8:c.295C= ENSP00000338009.4:p.Leu99=
ENST00000345378.6:c.1246C= ENSP00000223366.2:p.Leu416=
ENST00000395796.7:c.1240C= ENSP00000379142.3:p.Leu414=
ENST00000403799.7:c.1243C= ENSP00000384247.3:p.Leu415=
ENST00000437084.1:c.1192C= ENSP00000402840.1:p.Leu398=
ENST00000459642.1:n.623C=
ENST00000616242.4:c.1240C= ENSP00000482149.1:p.Leu414=
NM_000162.3:c.1243C= NP_000153.1:p.Leu415=
NM_033507.1:c.1246C= NP_277042.1:p.Leu416=
NM_033508.1:c.1240C= NP_277043.1:p.Leu414=
NM_000162.4:c.1243C= NP_000153.1:p.Leu415=
NM_001354800.1:c.1243C= NP_001341729.1:p.Leu415=
NM_001354801.1:c.232C= NP_001341730.1:p.Leu78=
NM_001354802.1:c.103C= NP_001341731.1:p.Leu35=
NM_001354803.1:c.277C= NP_001341732.1:p.Leu93=
NM_033507.2:c.1246C= NP_277042.1:p.Leu416=
NM_033508.2:c.1240C= NP_277043.1:p.Leu414=
XM_024446707.1:c.103C= XP_024302475.1:p.Leu35=
NM_000162.5:c.1243C= MANE Select NP_000153.1:p.Leu415=
NM_033507.3:c.1246C= NP_277042.1:p.Leu416=
NM_033508.3:c.1240C= NP_277043.1:p.Leu414=
NM_001354803.2:c.277C= NP_001341732.1:p.Leu93=