Canonical Allele Identifier: CA2832549755
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44149964dup , CM000669.2:g.44149964dup GRCh38
NC_000007.13:g.44189563dup , CM000669.1:g.44189563dup GRCh37
NC_000007.12:g.44156088dup NCBI36
NG_008847.1:g.44464dup
NG_008847.2:g.53211dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*577+9dup ENSP00000379142.4:n.*577+9dup
ENST00000616242.5:c.579+9dup ENSP00000482149.2:n.579+9dup
ENST00000682635.1:n.1065+9dup
ENST00000345378.7:c.582+9dup ENSP00000223366.2:n.582+9dup
ENST00000403799.8:c.579+9dup MANE Select ENSP00000384247.3:n.579+9dup
ENST00000671824.1:c.579+9dup ENSP00000500264.1:n.579+9dup
ENST00000673284.1:c.579+9dup ENSP00000499852.1:n.579+9dup
ENST00000345378.6:c.582+9dup ENSP00000223366.2:n.582+9dup
ENST00000395796.7:c.576+9dup ENSP00000379142.3:n.576+9dup
ENST00000403799.7:c.579+9dup ENSP00000384247.3:n.579+9dup
ENST00000437084.1:c.528+9dup ENSP00000402840.1:n.528+9dup
ENST00000616242.4:c.576+9dup ENSP00000482149.1:n.576+9dup
NM_000162.3:c.579+9dup NP_000153.1:n.579+9dup
NM_033507.1:c.582+9dup NP_277042.1:n.582+9dup
NM_033508.1:c.576+9dup NP_277043.1:n.576+9dup
NM_000162.4:c.579+9dup NP_000153.1:n.579+9dup
NM_001354800.1:c.579+9dup NP_001341729.1:n.579+9dup
NM_033507.2:c.582+9dup NP_277042.1:n.582+9dup
NM_033508.2:c.576+9dup NP_277043.1:n.576+9dup
NM_000162.5:c.579+9dup MANE Select NP_000153.1:n.579+9dup
NM_033507.3:c.582+9dup NP_277042.1:n.582+9dup
NM_033508.3:c.576+9dup NP_277043.1:n.576+9dup
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