Canonical Allele Identifier: CA367401719
Gene: GCK HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.44189634G>T (hg19) chr7:g.44150035G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44150035G>T , CM000669.2:g.44150035G>T GRCh38
NC_000007.13:g.44189634G>T , CM000669.1:g.44189634G>T GRCh37
NC_000007.12:g.44156159G>T NCBI36
NG_008847.1:g.44389C>A
NG_008847.2:g.53136C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*511C>A ENSP00000379142.4:n.*511C>A
ENST00000616242.5:c.513C>A ENSP00000482149.2:p.Phe171Leu
ENST00000682635.1:n.999C>A
ENST00000345378.7:c.516C>A ENSP00000223366.2:p.Phe172Leu
ENST00000403799.8:c.513C>A MANE Select ENSP00000384247.3:p.Phe171Leu
ENST00000671824.1:c.513C>A ENSP00000500264.1:p.Phe171Leu
ENST00000673284.1:c.513C>A ENSP00000499852.1:p.Phe171Leu
ENST00000345378.6:c.516C>A ENSP00000223366.2:p.Phe172Leu
ENST00000395796.7:c.510C>A ENSP00000379142.3:p.Phe170Leu
ENST00000403799.7:c.513C>A ENSP00000384247.3:p.Phe171Leu
ENST00000437084.1:c.462C>A ENSP00000402840.1:p.Phe154Leu
ENST00000616242.4:c.510C>A ENSP00000482149.1:p.Phe170Leu
NM_000162.3:c.513C>A NP_000153.1:p.Phe171Leu
NM_033507.1:c.516C>A NP_277042.1:p.Phe172Leu
NM_033508.1:c.510C>A NP_277043.1:p.Phe170Leu
NM_000162.4:c.513C>A NP_000153.1:p.Phe171Leu
NM_001354800.1:c.513C>A NP_001341729.1:p.Phe171Leu
NM_033507.2:c.516C>A NP_277042.1:p.Phe172Leu
NM_033508.2:c.510C>A NP_277043.1:p.Phe170Leu
NM_000162.5:c.513C>A MANE Select NP_000153.1:p.Phe171Leu
NM_033507.3:c.516C>A NP_277042.1:p.Phe172Leu
NM_033508.3:c.510C>A NP_277043.1:p.Phe170Leu
Search 100 bp 5'
Search 100 bp 3'