Canonical Allele Identifier: CA367398301
Gene: GCK HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.44185117G>T (hg19) chr7:g.44145518G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145518G>T , CM000669.2:g.44145518G>T GRCh38
NC_000007.13:g.44185117G>T , CM000669.1:g.44185117G>T GRCh37
NC_000007.12:g.44151642G>T NCBI36
NG_008847.1:g.48906C>A
NG_008847.2:g.57653C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1230C>A ENSP00000379142.4:n.*1230C>A
ENST00000616242.5:c.*352C>A ENSP00000482149.2:n.*352C>A
ENST00000683378.1:n.458C>A
ENST00000336642.9:c.266C>A ENSP00000338009.5:p.Ser89Tyr
ENST00000345378.7:c.1235C>A ENSP00000223366.2:p.Ser412Tyr
ENST00000403799.8:c.1232C>A MANE Select ENSP00000384247.3:p.Ser411Tyr
ENST00000671824.1:c.1295C>A ENSP00000500264.1:p.Ser432Tyr
ENST00000672743.1:n.244C>A
ENST00000673284.1:c.1232C>A ENSP00000499852.1:p.Ser411Tyr
ENST00000336642.8:c.284C>A ENSP00000338009.4:p.Ser95Tyr
ENST00000345378.6:c.1235C>A ENSP00000223366.2:p.Ser412Tyr
ENST00000395796.7:c.1229C>A ENSP00000379142.3:p.Ser410Tyr
ENST00000403799.7:c.1232C>A ENSP00000384247.3:p.Ser411Tyr
ENST00000437084.1:c.1181C>A ENSP00000402840.1:p.Ser394Tyr
ENST00000459642.1:n.612C>A
ENST00000616242.4:c.1229C>A ENSP00000482149.1:p.Ser410Tyr
NM_000162.3:c.1232C>A NP_000153.1:p.Ser411Tyr
NM_033507.1:c.1235C>A NP_277042.1:p.Ser412Tyr
NM_033508.1:c.1229C>A NP_277043.1:p.Ser410Tyr
NM_000162.4:c.1232C>A NP_000153.1:p.Ser411Tyr
NM_001354800.1:c.1232C>A NP_001341729.1:p.Ser411Tyr
NM_001354801.1:c.221C>A NP_001341730.1:p.Ser74Tyr
NM_001354802.1:c.92C>A NP_001341731.1:p.Ser31Tyr
NM_001354803.1:c.266C>A NP_001341732.1:p.Ser89Tyr
NM_033507.2:c.1235C>A NP_277042.1:p.Ser412Tyr
NM_033508.2:c.1229C>A NP_277043.1:p.Ser410Tyr
XM_024446707.1:c.92C>A XP_024302475.1:p.Ser31Tyr
NM_000162.5:c.1232C>A MANE Select NP_000153.1:p.Ser411Tyr
NM_033507.3:c.1235C>A NP_277042.1:p.Ser412Tyr
NM_033508.3:c.1229C>A NP_277043.1:p.Ser410Tyr
NM_001354803.2:c.266C>A NP_001341732.1:p.Ser89Tyr
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