Canonical Allele Identifier: CA367400398
Gene: GCK HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.44187249A>G (hg19) chr7:g.44147650A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44147650A>G , CM000669.2:g.44147650A>G GRCh38
NC_000007.13:g.44187249A>G , CM000669.1:g.44187249A>G GRCh37
NC_000007.12:g.44153774A>G NCBI36
NG_008847.1:g.46774T>C
NG_008847.2:g.55521T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*861T>C ENSP00000379142.4:n.*861T>C
ENST00000616242.5:c.853+10T>C ENSP00000482149.2:n.853+10T>C
ENST00000345378.7:c.866T>C ENSP00000223366.2:p.Leu289Pro
ENST00000403799.8:c.863T>C MANE Select ENSP00000384247.3:p.Leu288Pro
ENST00000671824.1:c.853+10T>C ENSP00000500264.1:n.853+10T>C
ENST00000673284.1:c.863T>C ENSP00000499852.1:p.Leu288Pro
ENST00000345378.6:c.866T>C ENSP00000223366.2:p.Leu289Pro
ENST00000395796.7:c.860T>C ENSP00000379142.3:p.Leu287Pro
ENST00000403799.7:c.863T>C ENSP00000384247.3:p.Leu288Pro
ENST00000437084.1:c.812T>C ENSP00000402840.1:p.Leu271Pro
ENST00000616242.4:c.860T>C ENSP00000482149.1:p.Leu287Pro
NM_000162.3:c.863T>C NP_000153.1:p.Leu288Pro
NM_033507.1:c.866T>C NP_277042.1:p.Leu289Pro
NM_033508.1:c.860T>C NP_277043.1:p.Leu287Pro
NM_000162.4:c.863T>C NP_000153.1:p.Leu288Pro
NM_001354800.1:c.863T>C NP_001341729.1:p.Leu288Pro
NM_033507.2:c.866T>C NP_277042.1:p.Leu289Pro
NM_033508.2:c.860T>C NP_277043.1:p.Leu287Pro
NM_000162.5:c.863T>C MANE Select NP_000153.1:p.Leu288Pro
NM_033507.3:c.866T>C NP_277042.1:p.Leu289Pro
NM_033508.3:c.860T>C NP_277043.1:p.Leu287Pro
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