Canonical Allele Identifier: CA2682574600
Gene: GCK HGNC NCBI

Linked Data

gnomAD v4: 7-44150145-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44150145G>T , CM000669.2:g.44150145G>T GRCh38
NC_000007.13:g.44189744G>T , CM000669.1:g.44189744G>T GRCh37
NC_000007.12:g.44156269G>T NCBI36
NG_008847.1:g.44279C>A
NG_008847.2:g.53026C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*482-81C>A ENSP00000379142.4:n.*482-81C>A
ENST00000616242.5:c.484-81C>A ENSP00000482149.2:n.484-81C>A
ENST00000682635.1:n.970-81C>A
ENST00000345378.7:c.487-81C>A ENSP00000223366.2:n.487-81C>A
ENST00000403799.8:c.484-81C>A MANE Select ENSP00000384247.3:n.484-81C>A
ENST00000671824.1:c.484-81C>A ENSP00000500264.1:n.484-81C>A
ENST00000673284.1:c.484-81C>A ENSP00000499852.1:n.484-81C>A
ENST00000345378.6:c.487-81C>A ENSP00000223366.2:n.487-81C>A
ENST00000395796.7:c.481-81C>A ENSP00000379142.3:n.481-81C>A
ENST00000403799.7:c.484-81C>A ENSP00000384247.3:n.484-81C>A
ENST00000437084.1:c.433-81C>A ENSP00000402840.1:n.433-81C>A
ENST00000616242.4:c.481-81C>A ENSP00000482149.1:n.481-81C>A
NM_000162.3:c.484-81C>A NP_000153.1:n.484-81C>A
NM_033507.1:c.487-81C>A NP_277042.1:n.487-81C>A
NM_033508.1:c.481-81C>A NP_277043.1:n.481-81C>A
NM_000162.4:c.484-81C>A NP_000153.1:n.484-81C>A
NM_001354800.1:c.484-81C>A NP_001341729.1:n.484-81C>A
NM_033507.2:c.487-81C>A NP_277042.1:n.487-81C>A
NM_033508.2:c.481-81C>A NP_277043.1:n.481-81C>A
NM_000162.5:c.484-81C>A MANE Select NP_000153.1:n.484-81C>A
NM_033507.3:c.487-81C>A NP_277042.1:n.487-81C>A
NM_033508.3:c.481-81C>A NP_277043.1:n.481-81C>A
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