Canonical Allele Identifier: CA367398264
Gene: GCK HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.44185111T>A (hg19) chr7:g.44145512T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145512T>A , CM000669.2:g.44145512T>A GRCh38
NC_000007.13:g.44185111T>A , CM000669.1:g.44185111T>A GRCh37
NC_000007.12:g.44151636T>A NCBI36
NG_008847.1:g.48912A>T
NG_008847.2:g.57659A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1236A>T ENSP00000379142.4:n.*1236A>T
ENST00000616242.5:c.*358A>T ENSP00000482149.2:n.*358A>T
ENST00000683378.1:n.464A>T
ENST00000336642.9:c.272A>T ENSP00000338009.5:p.Tyr91Phe
ENST00000345378.7:c.1241A>T ENSP00000223366.2:p.Tyr414Phe
ENST00000403799.8:c.1238A>T MANE Select ENSP00000384247.3:p.Tyr413Phe
ENST00000671824.1:c.1301A>T ENSP00000500264.1:p.Tyr434Phe
ENST00000672743.1:n.250A>T
ENST00000673284.1:c.1238A>T ENSP00000499852.1:p.Tyr413Phe
ENST00000336642.8:c.290A>T ENSP00000338009.4:p.Tyr97Phe
ENST00000345378.6:c.1241A>T ENSP00000223366.2:p.Tyr414Phe
ENST00000395796.7:c.1235A>T ENSP00000379142.3:p.Tyr412Phe
ENST00000403799.7:c.1238A>T ENSP00000384247.3:p.Tyr413Phe
ENST00000437084.1:c.1187A>T ENSP00000402840.1:p.Tyr396Phe
ENST00000459642.1:n.618A>T
ENST00000616242.4:c.1235A>T ENSP00000482149.1:p.Tyr412Phe
NM_000162.3:c.1238A>T NP_000153.1:p.Tyr413Phe
NM_033507.1:c.1241A>T NP_277042.1:p.Tyr414Phe
NM_033508.1:c.1235A>T NP_277043.1:p.Tyr412Phe
NM_000162.4:c.1238A>T NP_000153.1:p.Tyr413Phe
NM_001354800.1:c.1238A>T NP_001341729.1:p.Tyr413Phe
NM_001354801.1:c.227A>T NP_001341730.1:p.Tyr76Phe
NM_001354802.1:c.98A>T NP_001341731.1:p.Tyr33Phe
NM_001354803.1:c.272A>T NP_001341732.1:p.Tyr91Phe
NM_033507.2:c.1241A>T NP_277042.1:p.Tyr414Phe
NM_033508.2:c.1235A>T NP_277043.1:p.Tyr412Phe
XM_024446707.1:c.98A>T XP_024302475.1:p.Tyr33Phe
NM_000162.5:c.1238A>T MANE Select NP_000153.1:p.Tyr413Phe
NM_033507.3:c.1241A>T NP_277042.1:p.Tyr414Phe
NM_033508.3:c.1235A>T NP_277043.1:p.Tyr412Phe
NM_001354803.2:c.272A>T NP_001341732.1:p.Tyr91Phe
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