Canonical Allele Identifier: CA454863067
Gene: GCK HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.44185280G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145681G>A , CM000669.2:g.44145681G>A GRCh38
NC_000007.13:g.44185280G>A , CM000669.1:g.44185280G>A GRCh37
NC_000007.12:g.44151805G>A NCBI36
NG_008847.1:g.48743C>T
NG_008847.2:g.57490C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1067C>T ENSP00000379142.4:n.*1067C>T
ENST00000616242.5:c.*189C>T ENSP00000482149.2:n.*189C>T
ENST00000683378.1:n.295C>T
ENST00000336642.9:c.103C>T ENSP00000338009.5:p.Leu35=
ENST00000345378.7:c.1072C>T ENSP00000223366.2:p.Leu358=
ENST00000403799.8:c.1069C>T MANE Select ENSP00000384247.3:p.Leu357=
ENST00000671824.1:c.1132C>T ENSP00000500264.1:p.Leu378=
ENST00000672743.1:n.81C>T
ENST00000673284.1:c.1069C>T ENSP00000499852.1:p.Leu357=
ENST00000336642.8:c.121C>T ENSP00000338009.4:p.Leu41=
ENST00000345378.6:c.1072C>T ENSP00000223366.2:p.Leu358=
ENST00000395796.7:c.1066C>T ENSP00000379142.3:p.Leu356=
ENST00000403799.7:c.1069C>T ENSP00000384247.3:p.Leu357=
ENST00000437084.1:c.1018C>T ENSP00000402840.1:p.Leu340=
ENST00000459642.1:n.449C>T
ENST00000473353.1:n.367C>T
ENST00000616242.4:c.1066C>T ENSP00000482149.1:p.Leu356=
NM_000162.3:c.1069C>T NP_000153.1:p.Leu357=
NM_033507.1:c.1072C>T NP_277042.1:p.Leu358=
NM_033508.1:c.1066C>T NP_277043.1:p.Leu356=
NM_000162.4:c.1069C>T NP_000153.1:p.Leu357=
NM_001354800.1:c.1069C>T NP_001341729.1:p.Leu357=
NM_001354801.1:c.58C>T NP_001341730.1:p.Leu20=
NM_001354802.1:c.-72C>T NP_001341731.1:n.-72C>T
NM_001354803.1:c.103C>T NP_001341732.1:p.Leu35=
NM_033507.2:c.1072C>T NP_277042.1:p.Leu358=
NM_033508.2:c.1066C>T NP_277043.1:p.Leu356=
XM_024446707.1:c.-72C>T XP_024302475.1:n.-72C>T
NM_000162.5:c.1069C>T MANE Select NP_000153.1:p.Leu357=
NM_033507.3:c.1072C>T NP_277042.1:p.Leu358=
NM_033508.3:c.1066C>T NP_277043.1:p.Leu356=
NM_001354803.2:c.103C>T NP_001341732.1:p.Leu35=