Canonical Allele Identifier: CA157911599
Gene: GCK HGNC NCBI

Linked Data

dbSNP Id: rs762536430
gnomAD v3: 7-44144923-T-C
gnomAD v4: 7-44144923-T-C
MyVariant Identifiers: chr7:g.44184522T>C (hg19) chr7:g.44144923T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44144923T>C , CM000669.2:g.44144923T>C GRCh38
NC_000007.13:g.44184522T>C , CM000669.1:g.44184522T>C GRCh37
NC_000007.12:g.44151047T>C NCBI36
NG_008847.1:g.49501A>G
NG_008847.2:g.58248A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1609A>G ENSP00000379142.4:n.*1609A>G
ENST00000616242.5:c.*731A>G ENSP00000482149.2:n.*731A>G
ENST00000683378.1:n.837A>G
ENST00000336642.9:c.*213A>G ENSP00000338009.5:n.*213A>G
ENST00000345378.7:c.*213A>G ENSP00000223366.2:n.*213A>G
ENST00000403799.8:c.*213A>G MANE Select ENSP00000384247.3:n.*213A>G
ENST00000671824.1:c.*213A>G ENSP00000500264.1:n.*213A>G
ENST00000672743.1:n.381+242A>G
ENST00000673284.1:c.1369+242A>G ENSP00000499852.1:n.1369+242A>G
ENST00000336642.8:c.663A>G ENSP00000338009.4:n.663A>G
ENST00000345378.6:c.*213A>G ENSP00000223366.2:n.*213A>G
ENST00000395796.7:c.*213A>G ENSP00000379142.3:n.*213A>G
ENST00000403799.7:c.*213A>G ENSP00000384247.3:n.*213A>G
ENST00000459642.1:n.991A>G
ENST00000616242.4:c.1608A>G ENSP00000482149.1:n.1608A>G
NM_000162.3:c.*213A>G NP_000153.1:n.*213A>G
NM_033507.1:c.*213A>G NP_277042.1:n.*213A>G
NM_033508.1:c.*213A>G NP_277043.1:n.*213A>G
NM_000162.4:c.*213A>G NP_000153.1:n.*213A>G
NM_001354800.1:c.1369+242A>G NP_001341729.1:n.1369+242A>G
NM_001354801.1:c.*213A>G NP_001341730.1:n.*213A>G
NM_001354802.1:c.229+242A>G NP_001341731.1:n.229+242A>G
NM_001354803.1:c.*213A>G NP_001341732.1:n.*213A>G
NM_033507.2:c.*213A>G NP_277042.1:n.*213A>G
NM_033508.2:c.*213A>G NP_277043.1:n.*213A>G
XM_024446707.1:c.*213A>G XP_024302475.1:n.*213A>G
NM_000162.5:c.*213A>G MANE Select NP_000153.1:n.*213A>G
NM_033507.3:c.*213A>G NP_277042.1:n.*213A>G
NM_033508.3:c.*213A>G NP_277043.1:n.*213A>G
NM_001354803.2:c.*213A>G NP_001341732.1:n.*213A>G
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