Canonical Allele Identifier: CA367401990
Gene: GCK HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.44190605G>C (hg19) chr7:g.44151006G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44151006G>C , CM000669.2:g.44151006G>C GRCh38
NC_000007.13:g.44190605G>C , CM000669.1:g.44190605G>C GRCh37
NC_000007.12:g.44157130G>C NCBI36
NG_008847.1:g.43418C>G
NG_008847.2:g.52165C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*431C>G ENSP00000379142.4:n.*431C>G
ENST00000616242.5:c.433C>G ENSP00000482149.2:p.Pro145Ala
ENST00000682635.1:n.919C>G
ENST00000345378.7:c.436C>G ENSP00000223366.2:p.Pro146Ala
ENST00000403799.8:c.433C>G MANE Select ENSP00000384247.3:p.Pro145Ala
ENST00000671824.1:c.433C>G ENSP00000500264.1:p.Pro145Ala
ENST00000673284.1:c.433C>G ENSP00000499852.1:p.Pro145Ala
ENST00000345378.6:c.436C>G ENSP00000223366.2:p.Pro146Ala
ENST00000395796.7:c.430C>G ENSP00000379142.3:p.Pro144Ala
ENST00000403799.7:c.433C>G ENSP00000384247.3:p.Pro145Ala
ENST00000437084.1:c.382C>G ENSP00000402840.1:p.Pro128Ala
ENST00000616242.4:c.430C>G ENSP00000482149.1:p.Pro144Ala
NM_000162.3:c.433C>G NP_000153.1:p.Pro145Ala
NM_033507.1:c.436C>G NP_277042.1:p.Pro146Ala
NM_033508.1:c.430C>G NP_277043.1:p.Pro144Ala
NM_000162.4:c.433C>G NP_000153.1:p.Pro145Ala
NM_001354800.1:c.433C>G NP_001341729.1:p.Pro145Ala
NM_033507.2:c.436C>G NP_277042.1:p.Pro146Ala
NM_033508.2:c.430C>G NP_277043.1:p.Pro144Ala
NM_000162.5:c.433C>G MANE Select NP_000153.1:p.Pro145Ala
NM_033507.3:c.436C>G NP_277042.1:p.Pro146Ala
NM_033508.3:c.430C>G NP_277043.1:p.Pro144Ala
Search 100 bp 5'
Search 100 bp 3'