Canonical Allele Identifier: CA367399247
Gene: GCK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145698A>T , CM000669.2:g.44145698A>T GRCh38
NC_000007.13:g.44185297A>T , CM000669.1:g.44185297A>T GRCh37
NC_000007.12:g.44151822A>T NCBI36
NG_008847.1:g.48726T>A
NG_008847.2:g.57473T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1050T>A ENSP00000379142.4:n.*1050T>A
ENST00000616242.5:c.*172T>A ENSP00000482149.2:n.*172T>A
ENST00000683378.1:n.278T>A
ENST00000336642.9:c.86T>A ENSP00000338009.5:p.Ile29Asn
ENST00000345378.7:c.1055T>A ENSP00000223366.2:p.Ile352Asn
ENST00000403799.8:c.1052T>A MANE Select ENSP00000384247.3:p.Ile351Asn
ENST00000671824.1:c.1115T>A ENSP00000500264.1:p.Ile372Asn
ENST00000672743.1:n.64T>A
ENST00000673284.1:c.1052T>A ENSP00000499852.1:p.Ile351Asn
ENST00000336642.8:c.104T>A ENSP00000338009.4:p.Ile35Asn
ENST00000345378.6:c.1055T>A ENSP00000223366.2:p.Ile352Asn
ENST00000395796.7:c.1049T>A ENSP00000379142.3:p.Ile350Asn
ENST00000403799.7:c.1052T>A ENSP00000384247.3:p.Ile351Asn
ENST00000437084.1:c.1001T>A ENSP00000402840.1:p.Ile334Asn
ENST00000459642.1:n.432T>A
ENST00000473353.1:n.350T>A
ENST00000616242.4:c.1049T>A ENSP00000482149.1:p.Ile350Asn
NM_000162.3:c.1052T>A NP_000153.1:p.Ile351Asn
NM_033507.1:c.1055T>A NP_277042.1:p.Ile352Asn
NM_033508.1:c.1049T>A NP_277043.1:p.Ile350Asn
NM_000162.4:c.1052T>A NP_000153.1:p.Ile351Asn
NM_001354800.1:c.1052T>A NP_001341729.1:p.Ile351Asn
NM_001354801.1:c.41T>A NP_001341730.1:p.Ile14Asn
NM_001354802.1:c.-89T>A NP_001341731.1:n.-89T>A
NM_001354803.1:c.86T>A NP_001341732.1:p.Ile29Asn
NM_033507.2:c.1055T>A NP_277042.1:p.Ile352Asn
NM_033508.2:c.1049T>A NP_277043.1:p.Ile350Asn
XM_024446707.1:c.-89T>A XP_024302475.1:n.-89T>A
NM_000162.5:c.1052T>A MANE Select NP_000153.1:p.Ile351Asn
NM_033507.3:c.1055T>A NP_277042.1:p.Ile352Asn
NM_033508.3:c.1049T>A NP_277043.1:p.Ile350Asn
NM_001354803.2:c.86T>A NP_001341732.1:p.Ile29Asn