Canonical Allele Identifier: CA454608568
Gene: GCK HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.44187281C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44147682C>A , CM000669.2:g.44147682C>A GRCh38
NC_000007.13:g.44187281C>A , CM000669.1:g.44187281C>A GRCh37
NC_000007.12:g.44153806C>A NCBI36
NG_008847.1:g.46742G>T
NG_008847.2:g.55489G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*829G>T ENSP00000379142.4:n.*829G>T
ENST00000616242.5:c.831G>T ENSP00000482149.2:p.Val277=
ENST00000345378.7:c.834G>T ENSP00000223366.2:p.Val278=
ENST00000403799.8:c.831G>T MANE Select ENSP00000384247.3:p.Val277=
ENST00000671824.1:c.831G>T ENSP00000500264.1:p.Val277=
ENST00000673284.1:c.831G>T ENSP00000499852.1:p.Val277=
ENST00000345378.6:c.834G>T ENSP00000223366.2:p.Val278=
ENST00000395796.7:c.828G>T ENSP00000379142.3:p.Val276=
ENST00000403799.7:c.831G>T ENSP00000384247.3:p.Val277=
ENST00000437084.1:c.780G>T ENSP00000402840.1:p.Val260=
ENST00000616242.4:c.828G>T ENSP00000482149.1:p.Val276=
NM_000162.3:c.831G>T NP_000153.1:p.Val277=
NM_033507.1:c.834G>T NP_277042.1:p.Val278=
NM_033508.1:c.828G>T NP_277043.1:p.Val276=
XR_927223.1:n.16C>A
NM_000162.4:c.831G>T NP_000153.1:p.Val277=
NM_001354800.1:c.831G>T NP_001341729.1:p.Val277=
NM_033507.2:c.834G>T NP_277042.1:p.Val278=
NM_033508.2:c.828G>T NP_277043.1:p.Val276=
XR_927223.2:n.16C>A
NM_000162.5:c.831G>T MANE Select NP_000153.1:p.Val277=
NM_033507.3:c.834G>T NP_277042.1:p.Val278=
NM_033508.3:c.828G>T NP_277043.1:p.Val276=
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