Canonical Allele Identifier: CA367400521
Gene: GCK HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.44187307A>T (hg19) chr7:g.44147708A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44147708A>T , CM000669.2:g.44147708A>T GRCh38
NC_000007.13:g.44187307A>T , CM000669.1:g.44187307A>T GRCh37
NC_000007.12:g.44153832A>T NCBI36
NG_008847.1:g.46716T>A
NG_008847.2:g.55463T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*803T>A ENSP00000379142.4:n.*803T>A
ENST00000616242.5:c.805T>A ENSP00000482149.2:p.Phe269Ile
ENST00000345378.7:c.808T>A ENSP00000223366.2:p.Phe270Ile
ENST00000403799.8:c.805T>A MANE Select ENSP00000384247.3:p.Phe269Ile
ENST00000671824.1:c.805T>A ENSP00000500264.1:p.Phe269Ile
ENST00000673284.1:c.805T>A ENSP00000499852.1:p.Phe269Ile
ENST00000345378.6:c.808T>A ENSP00000223366.2:p.Phe270Ile
ENST00000395796.7:c.802T>A ENSP00000379142.3:p.Phe268Ile
ENST00000403799.7:c.805T>A ENSP00000384247.3:p.Phe269Ile
ENST00000437084.1:c.754T>A ENSP00000402840.1:p.Phe252Ile
ENST00000616242.4:c.802T>A ENSP00000482149.1:p.Phe268Ile
NM_000162.3:c.805T>A NP_000153.1:p.Phe269Ile
NM_033507.1:c.808T>A NP_277042.1:p.Phe270Ile
NM_033508.1:c.802T>A NP_277043.1:p.Phe268Ile
XR_927223.1:n.42A>T
NM_000162.4:c.805T>A NP_000153.1:p.Phe269Ile
NM_001354800.1:c.805T>A NP_001341729.1:p.Phe269Ile
NM_033507.2:c.808T>A NP_277042.1:p.Phe270Ile
NM_033508.2:c.802T>A NP_277043.1:p.Phe268Ile
XR_927223.2:n.42A>T
NM_000162.5:c.805T>A MANE Select NP_000153.1:p.Phe269Ile
NM_033507.3:c.808T>A NP_277042.1:p.Phe270Ile
NM_033508.3:c.802T>A NP_277043.1:p.Phe268Ile
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