Canonical Allele Identifier: CA454863109
Gene: GCK HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.44185113C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145514C>G , CM000669.2:g.44145514C>G GRCh38
NC_000007.13:g.44185113C>G , CM000669.1:g.44185113C>G GRCh37
NC_000007.12:g.44151638C>G NCBI36
NG_008847.1:g.48910G>C
NG_008847.2:g.57657G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1234G>C ENSP00000379142.4:n.*1234G>C
ENST00000616242.5:c.*356G>C ENSP00000482149.2:n.*356G>C
ENST00000683378.1:n.462G>C
ENST00000336642.9:c.270G>C ENSP00000338009.5:p.Val90=
ENST00000345378.7:c.1239G>C ENSP00000223366.2:p.Val413=
ENST00000403799.8:c.1236G>C MANE Select ENSP00000384247.3:p.Val412=
ENST00000671824.1:c.1299G>C ENSP00000500264.1:p.Val433=
ENST00000672743.1:n.248G>C
ENST00000673284.1:c.1236G>C ENSP00000499852.1:p.Val412=
ENST00000336642.8:c.288G>C ENSP00000338009.4:p.Val96=
ENST00000345378.6:c.1239G>C ENSP00000223366.2:p.Val413=
ENST00000395796.7:c.1233G>C ENSP00000379142.3:p.Val411=
ENST00000403799.7:c.1236G>C ENSP00000384247.3:p.Val412=
ENST00000437084.1:c.1185G>C ENSP00000402840.1:p.Val395=
ENST00000459642.1:n.616G>C
ENST00000616242.4:c.1233G>C ENSP00000482149.1:p.Val411=
NM_000162.3:c.1236G>C NP_000153.1:p.Val412=
NM_033507.1:c.1239G>C NP_277042.1:p.Val413=
NM_033508.1:c.1233G>C NP_277043.1:p.Val411=
NM_000162.4:c.1236G>C NP_000153.1:p.Val412=
NM_001354800.1:c.1236G>C NP_001341729.1:p.Val412=
NM_001354801.1:c.225G>C NP_001341730.1:p.Val75=
NM_001354802.1:c.96G>C NP_001341731.1:p.Val32=
NM_001354803.1:c.270G>C NP_001341732.1:p.Val90=
NM_033507.2:c.1239G>C NP_277042.1:p.Val413=
NM_033508.2:c.1233G>C NP_277043.1:p.Val411=
XM_024446707.1:c.96G>C XP_024302475.1:p.Val32=
NM_000162.5:c.1236G>C MANE Select NP_000153.1:p.Val412=
NM_033507.3:c.1239G>C NP_277042.1:p.Val413=
NM_033508.3:c.1233G>C NP_277043.1:p.Val411=
NM_001354803.2:c.270G>C NP_001341732.1:p.Val90=
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