Canonical Allele Identifier: CA1703612965
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145713T= , CM000669.2:g.44145713T= GRCh38
NC_000007.13:g.44185312T= , CM000669.1:g.44185312T= GRCh37
NC_000007.12:g.44151837T= NCBI36
NG_008847.1:g.48711A=
NG_008847.2:g.57458A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1035A= ENSP00000379142.4:n.*1035A=
ENST00000616242.5:c.*157A= ENSP00000482149.2:n.*157A=
ENST00000683378.1:n.263A=
ENST00000336642.9:c.71A= ENSP00000338009.5:p.Lys24=
ENST00000345378.7:c.1040A= ENSP00000223366.2:p.Lys347=
ENST00000403799.8:c.1037A= MANE Select ENSP00000384247.3:p.Lys346=
ENST00000671824.1:c.1100A= ENSP00000500264.1:p.Lys367=
ENST00000672743.1:n.49A=
ENST00000673284.1:c.1037A= ENSP00000499852.1:p.Lys346=
ENST00000336642.8:c.89A= ENSP00000338009.4:p.Lys30=
ENST00000345378.6:c.1040A= ENSP00000223366.2:p.Lys347=
ENST00000395796.7:c.1034A= ENSP00000379142.3:p.Lys345=
ENST00000403799.7:c.1037A= ENSP00000384247.3:p.Lys346=
ENST00000437084.1:c.986A= ENSP00000402840.1:p.Lys329=
ENST00000459642.1:n.417A=
ENST00000473353.1:n.335A=
ENST00000616242.4:c.1034A= ENSP00000482149.1:p.Lys345=
NM_000162.3:c.1037A= NP_000153.1:p.Lys346=
NM_033507.1:c.1040A= NP_277042.1:p.Lys347=
NM_033508.1:c.1034A= NP_277043.1:p.Lys345=
NM_000162.4:c.1037A= NP_000153.1:p.Lys346=
NM_001354800.1:c.1037A= NP_001341729.1:p.Lys346=
NM_001354801.1:c.26A= NP_001341730.1:p.Lys9=
NM_001354802.1:c.-104A= NP_001341731.1:n.-104A=
NM_001354803.1:c.71A= NP_001341732.1:p.Lys24=
NM_033507.2:c.1040A= NP_277042.1:p.Lys347=
NM_033508.2:c.1034A= NP_277043.1:p.Lys345=
XM_024446707.1:c.-104A= XP_024302475.1:n.-104A=
NM_000162.5:c.1037A= MANE Select NP_000153.1:p.Lys346=
NM_033507.3:c.1040A= NP_277042.1:p.Lys347=
NM_033508.3:c.1034A= NP_277043.1:p.Lys345=
NM_001354803.2:c.71A= NP_001341732.1:p.Lys24=