Canonical Allele Identifier: CA454863058
Gene: GCK HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.44185272G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145673G>A , CM000669.2:g.44145673G>A GRCh38
NC_000007.13:g.44185272G>A , CM000669.1:g.44185272G>A GRCh37
NC_000007.12:g.44151797G>A NCBI36
NG_008847.1:g.48751C>T
NG_008847.2:g.57498C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1075C>T ENSP00000379142.4:n.*1075C>T
ENST00000616242.5:c.*197C>T ENSP00000482149.2:n.*197C>T
ENST00000683378.1:n.303C>T
ENST00000336642.9:c.111C>T ENSP00000338009.5:p.Pro37=
ENST00000345378.7:c.1080C>T ENSP00000223366.2:p.Pro360=
ENST00000403799.8:c.1077C>T MANE Select ENSP00000384247.3:p.Pro359=
ENST00000671824.1:c.1140C>T ENSP00000500264.1:p.Pro380=
ENST00000672743.1:n.89C>T
ENST00000673284.1:c.1077C>T ENSP00000499852.1:p.Pro359=
ENST00000336642.8:c.129C>T ENSP00000338009.4:p.Pro43=
ENST00000345378.6:c.1080C>T ENSP00000223366.2:p.Pro360=
ENST00000395796.7:c.1074C>T ENSP00000379142.3:p.Pro358=
ENST00000403799.7:c.1077C>T ENSP00000384247.3:p.Pro359=
ENST00000437084.1:c.1026C>T ENSP00000402840.1:p.Pro342=
ENST00000459642.1:n.457C>T
ENST00000473353.1:n.375C>T
ENST00000616242.4:c.1074C>T ENSP00000482149.1:p.Pro358=
NM_000162.3:c.1077C>T NP_000153.1:p.Pro359=
NM_033507.1:c.1080C>T NP_277042.1:p.Pro360=
NM_033508.1:c.1074C>T NP_277043.1:p.Pro358=
NM_000162.4:c.1077C>T NP_000153.1:p.Pro359=
NM_001354800.1:c.1077C>T NP_001341729.1:p.Pro359=
NM_001354801.1:c.66C>T NP_001341730.1:p.Pro22=
NM_001354802.1:c.-64C>T NP_001341731.1:n.-64C>T
NM_001354803.1:c.111C>T NP_001341732.1:p.Pro37=
NM_033507.2:c.1080C>T NP_277042.1:p.Pro360=
NM_033508.2:c.1074C>T NP_277043.1:p.Pro358=
XM_024446707.1:c.-64C>T XP_024302475.1:n.-64C>T
NM_000162.5:c.1077C>T MANE Select NP_000153.1:p.Pro359=
NM_033507.3:c.1080C>T NP_277042.1:p.Pro360=
NM_033508.3:c.1074C>T NP_277043.1:p.Pro358=
NM_001354803.2:c.111C>T NP_001341732.1:p.Pro37=