Canonical Allele Identifier: CA2842717615
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44150062dup , CM000669.2:g.44150062dup GRCh38
NC_000007.13:g.44189661dup , CM000669.1:g.44189661dup GRCh37
NC_000007.12:g.44156186dup NCBI36
NG_008847.1:g.44362dup
NG_008847.2:g.53109dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*484dup ENSP00000379142.4:n.*484dup
ENST00000616242.5:c.486dup ENSP00000482149.2:p.Ile163HisfsTer?
ENST00000682635.1:n.972dup
ENST00000345378.7:c.489dup ENSP00000223366.2:p.Ile164HisfsTer?
ENST00000403799.8:c.486dup MANE Select ENSP00000384247.3:p.Ile163HisfsTer?
ENST00000671824.1:c.486dup ENSP00000500264.1:p.Ile163HisfsTer?
ENST00000673284.1:c.486dup ENSP00000499852.1:p.Ile163HisfsTer?
ENST00000345378.6:c.489dup ENSP00000223366.2:p.Ile164HisfsTer?
ENST00000395796.7:c.483dup ENSP00000379142.3:p.Ile162HisfsTer?
ENST00000403799.7:c.486dup ENSP00000384247.3:p.Ile163HisfsTer?
ENST00000437084.1:c.435dup ENSP00000402840.1:p.Ile146HisfsTer?
ENST00000616242.4:c.483dup ENSP00000482149.1:p.Ile162HisfsTer?
NM_000162.3:c.486dup NP_000153.1:p.Ile163HisfsTer?
NM_033507.1:c.489dup NP_277042.1:p.Ile164HisfsTer?
NM_033508.1:c.483dup NP_277043.1:p.Ile162HisfsTer?
NM_000162.4:c.486dup NP_000153.1:p.Ile163HisfsTer?
NM_001354800.1:c.486dup NP_001341729.1:p.Ile163HisfsTer?
NM_033507.2:c.489dup NP_277042.1:p.Ile164HisfsTer?
NM_033508.2:c.483dup NP_277043.1:p.Ile162HisfsTer?
NM_000162.5:c.486dup MANE Select NP_000153.1:p.Ile163HisfsTer?
NM_033507.3:c.489dup NP_277042.1:p.Ile164HisfsTer?
NM_033508.3:c.483dup NP_277043.1:p.Ile162HisfsTer?
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