Canonical Allele Identifier: CA454608764
Gene: GCK HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.44187419A>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44147820A>G , CM000669.2:g.44147820A>G GRCh38
NC_000007.13:g.44187419A>G , CM000669.1:g.44187419A>G GRCh37
NC_000007.12:g.44153944A>G NCBI36
NG_008847.1:g.46604T>C
NG_008847.2:g.55351T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*691T>C ENSP00000379142.4:n.*691T>C
ENST00000616242.5:c.693T>C ENSP00000482149.2:p.Asn231=
ENST00000345378.7:c.696T>C ENSP00000223366.2:p.Asn232=
ENST00000403799.8:c.693T>C MANE Select ENSP00000384247.3:p.Asn231=
ENST00000671824.1:c.693T>C ENSP00000500264.1:p.Asn231=
ENST00000673284.1:c.693T>C ENSP00000499852.1:p.Asn231=
ENST00000345378.6:c.696T>C ENSP00000223366.2:p.Asn232=
ENST00000395796.7:c.690T>C ENSP00000379142.3:p.Asn230=
ENST00000403799.7:c.693T>C ENSP00000384247.3:p.Asn231=
ENST00000437084.1:c.642T>C ENSP00000402840.1:p.Asn214=
ENST00000616242.4:c.690T>C ENSP00000482149.1:p.Asn230=
NM_000162.3:c.693T>C NP_000153.1:p.Asn231=
NM_033507.1:c.696T>C NP_277042.1:p.Asn232=
NM_033508.1:c.690T>C NP_277043.1:p.Asn230=
XR_927223.1:n.82+72A>G
NM_000162.4:c.693T>C NP_000153.1:p.Asn231=
NM_001354800.1:c.693T>C NP_001341729.1:p.Asn231=
NM_033507.2:c.696T>C NP_277042.1:p.Asn232=
NM_033508.2:c.690T>C NP_277043.1:p.Asn230=
XR_927223.2:n.82+72A>G
NM_000162.5:c.693T>C MANE Select NP_000153.1:p.Asn231=
NM_033507.3:c.696T>C NP_277042.1:p.Asn232=
NM_033508.3:c.690T>C NP_277043.1:p.Asn230=
Search 100 bp 5'
Search 100 bp 3'