Canonical Allele Identifier: CA2842717612
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44149983dup , CM000669.2:g.44149983dup GRCh38
NC_000007.13:g.44189582dup , CM000669.1:g.44189582dup GRCh37
NC_000007.12:g.44156107dup NCBI36
NG_008847.1:g.44441dup
NG_008847.2:g.53188dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*563dup ENSP00000379142.4:n.*563dup
ENST00000616242.5:c.565dup ENSP00000482149.2:p.Ile189AsnfsTer8
ENST00000682635.1:n.1051dup
ENST00000345378.7:c.568dup ENSP00000223366.2:p.Ile190AsnfsTer8
ENST00000403799.8:c.565dup MANE Select ENSP00000384247.3:p.Ile189AsnfsTer8
ENST00000671824.1:c.565dup ENSP00000500264.1:p.Ile189AsnfsTer8
ENST00000673284.1:c.565dup ENSP00000499852.1:p.Ile189AsnfsTer8
ENST00000345378.6:c.568dup ENSP00000223366.2:p.Ile190AsnfsTer8
ENST00000395796.7:c.562dup ENSP00000379142.3:p.Ile188AsnfsTer8
ENST00000403799.7:c.565dup ENSP00000384247.3:p.Ile189AsnfsTer8
ENST00000437084.1:c.514dup ENSP00000402840.1:p.Ile172AsnfsTer8
ENST00000616242.4:c.562dup ENSP00000482149.1:p.Ile188AsnfsTer8
NM_000162.3:c.565dup NP_000153.1:p.Ile189AsnfsTer8
NM_033507.1:c.568dup NP_277042.1:p.Ile190AsnfsTer8
NM_033508.1:c.562dup NP_277043.1:p.Ile188AsnfsTer8
NM_000162.4:c.565dup NP_000153.1:p.Ile189AsnfsTer8
NM_001354800.1:c.565dup NP_001341729.1:p.Ile189AsnfsTer8
NM_033507.2:c.568dup NP_277042.1:p.Ile190AsnfsTer8
NM_033508.2:c.562dup NP_277043.1:p.Ile188AsnfsTer8
NM_000162.5:c.565dup MANE Select NP_000153.1:p.Ile189AsnfsTer8
NM_033507.3:c.568dup NP_277042.1:p.Ile190AsnfsTer8
NM_033508.3:c.562dup NP_277043.1:p.Ile188AsnfsTer8
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