Canonical Allele Identifier: CA367402157
Gene: GCK HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.44190652C>G (hg19) chr7:g.44151053C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44151053C>G , CM000669.2:g.44151053C>G GRCh38
NC_000007.13:g.44190652C>G , CM000669.1:g.44190652C>G GRCh37
NC_000007.12:g.44157177C>G NCBI36
NG_008847.1:g.43371G>C
NG_008847.2:g.52118G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*384G>C ENSP00000379142.4:n.*384G>C
ENST00000616242.5:c.386G>C ENSP00000482149.2:p.Cys129Ser
ENST00000682635.1:n.872G>C
ENST00000345378.7:c.389G>C ENSP00000223366.2:p.Cys130Ser
ENST00000403799.8:c.386G>C MANE Select ENSP00000384247.3:p.Cys129Ser
ENST00000671824.1:c.386G>C ENSP00000500264.1:p.Cys129Ser
ENST00000673284.1:c.386G>C ENSP00000499852.1:p.Cys129Ser
ENST00000345378.6:c.389G>C ENSP00000223366.2:p.Cys130Ser
ENST00000395796.7:c.383G>C ENSP00000379142.3:p.Cys128Ser
ENST00000403799.7:c.386G>C ENSP00000384247.3:p.Cys129Ser
ENST00000437084.1:c.364-29G>C ENSP00000402840.1:n.364-29G>C
ENST00000616242.4:c.383G>C ENSP00000482149.1:p.Cys128Ser
NM_000162.3:c.386G>C NP_000153.1:p.Cys129Ser
NM_033507.1:c.389G>C NP_277042.1:p.Cys130Ser
NM_033508.1:c.383G>C NP_277043.1:p.Cys128Ser
NM_000162.4:c.386G>C NP_000153.1:p.Cys129Ser
NM_001354800.1:c.386G>C NP_001341729.1:p.Cys129Ser
NM_033507.2:c.389G>C NP_277042.1:p.Cys130Ser
NM_033508.2:c.383G>C NP_277043.1:p.Cys128Ser
NM_000162.5:c.386G>C MANE Select NP_000153.1:p.Cys129Ser
NM_033507.3:c.389G>C NP_277042.1:p.Cys130Ser
NM_033508.3:c.383G>C NP_277043.1:p.Cys128Ser
Search 100 bp 5'
Search 100 bp 3'