Canonical Allele Identifier: CA454609873
Gene: GCK HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.44190657A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44151058A>G , CM000669.2:g.44151058A>G GRCh38
NC_000007.13:g.44190657A>G , CM000669.1:g.44190657A>G GRCh37
NC_000007.12:g.44157182A>G NCBI36
NG_008847.1:g.43366T>C
NG_008847.2:g.52113T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*379T>C ENSP00000379142.4:n.*379T>C
ENST00000616242.5:c.381T>C ENSP00000482149.2:p.Ser127=
ENST00000682635.1:n.867T>C
ENST00000345378.7:c.384T>C ENSP00000223366.2:p.Ser128=
ENST00000403799.8:c.381T>C MANE Select ENSP00000384247.3:p.Ser127=
ENST00000671824.1:c.381T>C ENSP00000500264.1:p.Ser127=
ENST00000673284.1:c.381T>C ENSP00000499852.1:p.Ser127=
ENST00000345378.6:c.384T>C ENSP00000223366.2:p.Ser128=
ENST00000395796.7:c.378T>C ENSP00000379142.3:p.Ser126=
ENST00000403799.7:c.381T>C ENSP00000384247.3:p.Ser127=
ENST00000437084.1:c.364-34T>C ENSP00000402840.1:n.364-34T>C
ENST00000616242.4:c.378T>C ENSP00000482149.1:p.Ser126=
NM_000162.3:c.381T>C NP_000153.1:p.Ser127=
NM_033507.1:c.384T>C NP_277042.1:p.Ser128=
NM_033508.1:c.378T>C NP_277043.1:p.Ser126=
NM_000162.4:c.381T>C NP_000153.1:p.Ser127=
NM_001354800.1:c.381T>C NP_001341729.1:p.Ser127=
NM_033507.2:c.384T>C NP_277042.1:p.Ser128=
NM_033508.2:c.378T>C NP_277043.1:p.Ser126=
NM_000162.5:c.381T>C MANE Select NP_000153.1:p.Ser127=
NM_033507.3:c.384T>C NP_277042.1:p.Ser128=
NM_033508.3:c.378T>C NP_277043.1:p.Ser126=
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