Canonical Allele Identifier: CA367401288
Gene: GCK HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.44189406A>C (hg19) chr7:g.44149807A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44149807A>C , CM000669.2:g.44149807A>C GRCh38
NC_000007.13:g.44189406A>C , CM000669.1:g.44189406A>C GRCh37
NC_000007.12:g.44155931A>C NCBI36
NG_008847.1:g.44617T>G
NG_008847.2:g.53364T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*630T>G ENSP00000379142.4:n.*630T>G
ENST00000616242.5:c.632T>G ENSP00000482149.2:p.Ile211Ser
ENST00000682635.1:n.1118T>G
ENST00000345378.7:c.635T>G ENSP00000223366.2:p.Ile212Ser
ENST00000403799.8:c.632T>G MANE Select ENSP00000384247.3:p.Ile211Ser
ENST00000671824.1:c.632T>G ENSP00000500264.1:p.Ile211Ser
ENST00000673284.1:c.632T>G ENSP00000499852.1:p.Ile211Ser
ENST00000345378.6:c.635T>G ENSP00000223366.2:p.Ile212Ser
ENST00000395796.7:c.629T>G ENSP00000379142.3:p.Ile210Ser
ENST00000403799.7:c.632T>G ENSP00000384247.3:p.Ile211Ser
ENST00000437084.1:c.581T>G ENSP00000402840.1:p.Ile194Ser
ENST00000616242.4:c.629T>G ENSP00000482149.1:p.Ile210Ser
NM_000162.3:c.632T>G NP_000153.1:p.Ile211Ser
NM_033507.1:c.635T>G NP_277042.1:p.Ile212Ser
NM_033508.1:c.629T>G NP_277043.1:p.Ile210Ser
NM_000162.4:c.632T>G NP_000153.1:p.Ile211Ser
NM_001354800.1:c.632T>G NP_001341729.1:p.Ile211Ser
NM_033507.2:c.635T>G NP_277042.1:p.Ile212Ser
NM_033508.2:c.629T>G NP_277043.1:p.Ile210Ser
NM_000162.5:c.632T>G MANE Select NP_000153.1:p.Ile211Ser
NM_033507.3:c.635T>G NP_277042.1:p.Ile212Ser
NM_033508.3:c.629T>G NP_277043.1:p.Ile210Ser
Search 100 bp 5'
Search 100 bp 3'