Canonical Allele Identifier: CA1703612847
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145505C= , CM000669.2:g.44145505C= GRCh38
NC_000007.13:g.44185104C= , CM000669.1:g.44185104C= GRCh37
NC_000007.12:g.44151629C= NCBI36
NG_008847.1:g.48919G=
NG_008847.2:g.57666G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1243G= ENSP00000379142.4:n.*1243G=
ENST00000616242.5:c.*365G= ENSP00000482149.2:n.*365G=
ENST00000683378.1:n.471G=
ENST00000336642.9:c.279G= ENSP00000338009.5:p.Leu93=
ENST00000345378.7:c.1248G= ENSP00000223366.2:p.Leu416=
ENST00000403799.8:c.1245G= MANE Select ENSP00000384247.3:p.Leu415=
ENST00000671824.1:c.1308G= ENSP00000500264.1:p.Leu436=
ENST00000672743.1:n.257G=
ENST00000673284.1:c.1245G= ENSP00000499852.1:p.Leu415=
ENST00000336642.8:c.297G= ENSP00000338009.4:p.Leu99=
ENST00000345378.6:c.1248G= ENSP00000223366.2:p.Leu416=
ENST00000395796.7:c.1242G= ENSP00000379142.3:p.Leu414=
ENST00000403799.7:c.1245G= ENSP00000384247.3:p.Leu415=
ENST00000437084.1:c.1194G= ENSP00000402840.1:p.Leu398=
ENST00000459642.1:n.625G=
ENST00000616242.4:c.1242G= ENSP00000482149.1:p.Leu414=
NM_000162.3:c.1245G= NP_000153.1:p.Leu415=
NM_033507.1:c.1248G= NP_277042.1:p.Leu416=
NM_033508.1:c.1242G= NP_277043.1:p.Leu414=
NM_000162.4:c.1245G= NP_000153.1:p.Leu415=
NM_001354800.1:c.1245G= NP_001341729.1:p.Leu415=
NM_001354801.1:c.234G= NP_001341730.1:p.Leu78=
NM_001354802.1:c.105G= NP_001341731.1:p.Leu35=
NM_001354803.1:c.279G= NP_001341732.1:p.Leu93=
NM_033507.2:c.1248G= NP_277042.1:p.Leu416=
NM_033508.2:c.1242G= NP_277043.1:p.Leu414=
XM_024446707.1:c.105G= XP_024302475.1:p.Leu35=
NM_000162.5:c.1245G= MANE Select NP_000153.1:p.Leu415=
NM_033507.3:c.1248G= NP_277042.1:p.Leu416=
NM_033508.3:c.1242G= NP_277043.1:p.Leu414=
NM_001354803.2:c.279G= NP_001341732.1:p.Leu93=