Canonical Allele Identifier: CA838781124
Gene: GCK HGNC NCBI

Linked Data

dbSNP Id: rs1399606597
MyVariant Identifiers: chr7:g.44189806T>A (hg19) chr7:g.44150207T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44150207T>A , CM000669.2:g.44150207T>A GRCh38
NC_000007.13:g.44189806T>A , CM000669.1:g.44189806T>A GRCh37
NC_000007.12:g.44156331T>A NCBI36
NG_008847.1:g.44217A>T
NG_008847.2:g.52964A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*482-143A>T ENSP00000379142.4:n.*482-143A>T
ENST00000616242.5:c.484-143A>T ENSP00000482149.2:n.484-143A>T
ENST00000682635.1:n.970-143A>T
ENST00000345378.7:c.487-143A>T ENSP00000223366.2:n.487-143A>T
ENST00000403799.8:c.484-143A>T MANE Select ENSP00000384247.3:n.484-143A>T
ENST00000671824.1:c.484-143A>T ENSP00000500264.1:n.484-143A>T
ENST00000673284.1:c.484-143A>T ENSP00000499852.1:n.484-143A>T
ENST00000345378.6:c.487-143A>T ENSP00000223366.2:n.487-143A>T
ENST00000395796.7:c.481-143A>T ENSP00000379142.3:n.481-143A>T
ENST00000403799.7:c.484-143A>T ENSP00000384247.3:n.484-143A>T
ENST00000437084.1:c.433-143A>T ENSP00000402840.1:n.433-143A>T
ENST00000616242.4:c.481-143A>T ENSP00000482149.1:n.481-143A>T
NM_000162.3:c.484-143A>T NP_000153.1:n.484-143A>T
NM_033507.1:c.487-143A>T NP_277042.1:n.487-143A>T
NM_033508.1:c.481-143A>T NP_277043.1:n.481-143A>T
NM_000162.4:c.484-143A>T NP_000153.1:n.484-143A>T
NM_001354800.1:c.484-143A>T NP_001341729.1:n.484-143A>T
NM_033507.2:c.487-143A>T NP_277042.1:n.487-143A>T
NM_033508.2:c.481-143A>T NP_277043.1:n.481-143A>T
NM_000162.5:c.484-143A>T MANE Select NP_000153.1:n.484-143A>T
NM_033507.3:c.487-143A>T NP_277042.1:n.487-143A>T
NM_033508.3:c.481-143A>T NP_277043.1:n.481-143A>T
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