Canonical Allele Identifier: CA367401975
Gene: GCK HGNC NCBI

Linked Data

gnomAD v4: 7-44151000-C-T
MyVariant Identifiers: chr7:g.44190599C>T (hg19) chr7:g.44151000C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44151000C>T , CM000669.2:g.44151000C>T GRCh38
NC_000007.13:g.44190599C>T , CM000669.1:g.44190599C>T GRCh37
NC_000007.12:g.44157124C>T NCBI36
NG_008847.1:g.43424G>A
NG_008847.2:g.52171G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*437G>A ENSP00000379142.4:n.*437G>A
ENST00000616242.5:c.439G>A ENSP00000482149.2:p.Gly147Ser
ENST00000682635.1:n.925G>A
ENST00000345378.7:c.442G>A ENSP00000223366.2:p.Gly148Ser
ENST00000403799.8:c.439G>A MANE Select ENSP00000384247.3:p.Gly147Ser
ENST00000671824.1:c.439G>A ENSP00000500264.1:p.Gly147Ser
ENST00000673284.1:c.439G>A ENSP00000499852.1:p.Gly147Ser
ENST00000345378.6:c.442G>A ENSP00000223366.2:p.Gly148Ser
ENST00000395796.7:c.436G>A ENSP00000379142.3:p.Gly146Ser
ENST00000403799.7:c.439G>A ENSP00000384247.3:p.Gly147Ser
ENST00000437084.1:c.388G>A ENSP00000402840.1:p.Gly130Ser
ENST00000616242.4:c.436G>A ENSP00000482149.1:p.Gly146Ser
NM_000162.3:c.439G>A NP_000153.1:p.Gly147Ser
NM_033507.1:c.442G>A NP_277042.1:p.Gly148Ser
NM_033508.1:c.436G>A NP_277043.1:p.Gly146Ser
NM_000162.4:c.439G>A NP_000153.1:p.Gly147Ser
NM_001354800.1:c.439G>A NP_001341729.1:p.Gly147Ser
NM_033507.2:c.442G>A NP_277042.1:p.Gly148Ser
NM_033508.2:c.436G>A NP_277043.1:p.Gly146Ser
NM_000162.5:c.439G>A MANE Select NP_000153.1:p.Gly147Ser
NM_033507.3:c.442G>A NP_277042.1:p.Gly148Ser
NM_033508.3:c.436G>A NP_277043.1:p.Gly146Ser
Search 100 bp 5'
Search 100 bp 3'