Canonical Allele Identifier: CA213808
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36232
ClinVar RCV Id: RCV000029895 RCV002463602 RCV003883123
dbSNP Id: rs193922310
MyVariant Identifiers: chr7:g.44189434T>C (hg19) chr7:g.44149835T>C (hg38)
ERepo: CA213808/MONDO:0015967/086
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44149835T>C , CM000669.2:g.44149835T>C GRCh38
NC_000007.13:g.44189434T>C , CM000669.1:g.44189434T>C GRCh37
NC_000007.12:g.44155959T>C NCBI36
NG_008847.1:g.44589A>G
NG_008847.2:g.53336A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*602A>G ENSP00000379142.4:n.*602A>G
ENST00000616242.5:c.604A>G ENSP00000482149.2:p.Met202Val
ENST00000682635.1:n.1090A>G
ENST00000345378.7:c.607A>G ENSP00000223366.2:p.Met203Val
ENST00000403799.8:c.604A>G MANE Select ENSP00000384247.3:p.Met202Val
ENST00000671824.1:c.604A>G ENSP00000500264.1:p.Met202Val
ENST00000673284.1:c.604A>G ENSP00000499852.1:p.Met202Val
ENST00000345378.6:c.607A>G ENSP00000223366.2:p.Met203Val
ENST00000395796.7:c.601A>G ENSP00000379142.3:p.Met201Val
ENST00000403799.7:c.604A>G ENSP00000384247.3:p.Met202Val
ENST00000437084.1:c.553A>G ENSP00000402840.1:p.Met185Val
ENST00000616242.4:c.601A>G ENSP00000482149.1:p.Met201Val
NM_000162.3:c.604A>G NP_000153.1:p.Met202Val
NM_033507.1:c.607A>G NP_277042.1:p.Met203Val
NM_033508.1:c.601A>G NP_277043.1:p.Met201Val
NM_000162.4:c.604A>G NP_000153.1:p.Met202Val
NM_001354800.1:c.604A>G NP_001341729.1:p.Met202Val
NM_033507.2:c.607A>G NP_277042.1:p.Met203Val
NM_033508.2:c.601A>G NP_277043.1:p.Met201Val
NM_000162.5:c.604A>G MANE Select NP_000153.1:p.Met202Val
NM_033507.3:c.607A>G NP_277042.1:p.Met203Val
NM_033508.3:c.601A>G NP_277043.1:p.Met201Val
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