Canonical Allele Identifier: CA367398307
Gene: GCK HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.44185118A>T (hg19) chr7:g.44145519A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145519A>T , CM000669.2:g.44145519A>T GRCh38
NC_000007.13:g.44185118A>T , CM000669.1:g.44185118A>T GRCh37
NC_000007.12:g.44151643A>T NCBI36
NG_008847.1:g.48905T>A
NG_008847.2:g.57652T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1229T>A ENSP00000379142.4:n.*1229T>A
ENST00000616242.5:c.*351T>A ENSP00000482149.2:n.*351T>A
ENST00000683378.1:n.457T>A
ENST00000336642.9:c.265T>A ENSP00000338009.5:p.Ser89Thr
ENST00000345378.7:c.1234T>A ENSP00000223366.2:p.Ser412Thr
ENST00000403799.8:c.1231T>A MANE Select ENSP00000384247.3:p.Ser411Thr
ENST00000671824.1:c.1294T>A ENSP00000500264.1:p.Ser432Thr
ENST00000672743.1:n.243T>A
ENST00000673284.1:c.1231T>A ENSP00000499852.1:p.Ser411Thr
ENST00000336642.8:c.283T>A ENSP00000338009.4:p.Ser95Thr
ENST00000345378.6:c.1234T>A ENSP00000223366.2:p.Ser412Thr
ENST00000395796.7:c.1228T>A ENSP00000379142.3:p.Ser410Thr
ENST00000403799.7:c.1231T>A ENSP00000384247.3:p.Ser411Thr
ENST00000437084.1:c.1180T>A ENSP00000402840.1:p.Ser394Thr
ENST00000459642.1:n.611T>A
ENST00000616242.4:c.1228T>A ENSP00000482149.1:p.Ser410Thr
NM_000162.3:c.1231T>A NP_000153.1:p.Ser411Thr
NM_033507.1:c.1234T>A NP_277042.1:p.Ser412Thr
NM_033508.1:c.1228T>A NP_277043.1:p.Ser410Thr
NM_000162.4:c.1231T>A NP_000153.1:p.Ser411Thr
NM_001354800.1:c.1231T>A NP_001341729.1:p.Ser411Thr
NM_001354801.1:c.220T>A NP_001341730.1:p.Ser74Thr
NM_001354802.1:c.91T>A NP_001341731.1:p.Ser31Thr
NM_001354803.1:c.265T>A NP_001341732.1:p.Ser89Thr
NM_033507.2:c.1234T>A NP_277042.1:p.Ser412Thr
NM_033508.2:c.1228T>A NP_277043.1:p.Ser410Thr
XM_024446707.1:c.91T>A XP_024302475.1:p.Ser31Thr
NM_000162.5:c.1231T>A MANE Select NP_000153.1:p.Ser411Thr
NM_033507.3:c.1234T>A NP_277042.1:p.Ser412Thr
NM_033508.3:c.1228T>A NP_277043.1:p.Ser410Thr
NM_001354803.2:c.265T>A NP_001341732.1:p.Ser89Thr
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