Canonical Allele Identifier: CA367399299
Gene: GCK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145707A>T , CM000669.2:g.44145707A>T GRCh38
NC_000007.13:g.44185306A>T , CM000669.1:g.44185306A>T GRCh37
NC_000007.12:g.44151831A>T NCBI36
NG_008847.1:g.48717T>A
NG_008847.2:g.57464T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1041T>A ENSP00000379142.4:n.*1041T>A
ENST00000616242.5:c.*163T>A ENSP00000482149.2:n.*163T>A
ENST00000683378.1:n.269T>A
ENST00000336642.9:c.77T>A ENSP00000338009.5:p.Ile26Asn
ENST00000345378.7:c.1046T>A ENSP00000223366.2:p.Ile349Asn
ENST00000403799.8:c.1043T>A MANE Select ENSP00000384247.3:p.Ile348Asn
ENST00000671824.1:c.1106T>A ENSP00000500264.1:p.Ile369Asn
ENST00000672743.1:n.55T>A
ENST00000673284.1:c.1043T>A ENSP00000499852.1:p.Ile348Asn
ENST00000336642.8:c.95T>A ENSP00000338009.4:p.Ile32Asn
ENST00000345378.6:c.1046T>A ENSP00000223366.2:p.Ile349Asn
ENST00000395796.7:c.1040T>A ENSP00000379142.3:p.Ile347Asn
ENST00000403799.7:c.1043T>A ENSP00000384247.3:p.Ile348Asn
ENST00000437084.1:c.992T>A ENSP00000402840.1:p.Ile331Asn
ENST00000459642.1:n.423T>A
ENST00000473353.1:n.341T>A
ENST00000616242.4:c.1040T>A ENSP00000482149.1:p.Ile347Asn
NM_000162.3:c.1043T>A NP_000153.1:p.Ile348Asn
NM_033507.1:c.1046T>A NP_277042.1:p.Ile349Asn
NM_033508.1:c.1040T>A NP_277043.1:p.Ile347Asn
NM_000162.4:c.1043T>A NP_000153.1:p.Ile348Asn
NM_001354800.1:c.1043T>A NP_001341729.1:p.Ile348Asn
NM_001354801.1:c.32T>A NP_001341730.1:p.Ile11Asn
NM_001354802.1:c.-98T>A NP_001341731.1:n.-98T>A
NM_001354803.1:c.77T>A NP_001341732.1:p.Ile26Asn
NM_033507.2:c.1046T>A NP_277042.1:p.Ile349Asn
NM_033508.2:c.1040T>A NP_277043.1:p.Ile347Asn
XM_024446707.1:c.-98T>A XP_024302475.1:n.-98T>A
NM_000162.5:c.1043T>A MANE Select NP_000153.1:p.Ile348Asn
NM_033507.3:c.1046T>A NP_277042.1:p.Ile349Asn
NM_033508.3:c.1040T>A NP_277043.1:p.Ile347Asn
NM_001354803.2:c.77T>A NP_001341732.1:p.Ile26Asn