Canonical Allele Identifier: CA367398788
Gene: GCK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145612G>T , CM000669.2:g.44145612G>T GRCh38
NC_000007.13:g.44185211G>T , CM000669.1:g.44185211G>T GRCh37
NC_000007.12:g.44151736G>T NCBI36
NG_008847.1:g.48812C>A
NG_008847.2:g.57559C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1136C>A ENSP00000379142.4:n.*1136C>A
ENST00000616242.5:c.*258C>A ENSP00000482149.2:n.*258C>A
ENST00000683378.1:n.364C>A
ENST00000336642.9:c.172C>A ENSP00000338009.5:p.His58Asn
ENST00000345378.7:c.1141C>A ENSP00000223366.2:p.His381Asn
ENST00000403799.8:c.1138C>A MANE Select ENSP00000384247.3:p.His380Asn
ENST00000671824.1:c.1201C>A ENSP00000500264.1:p.His401Asn
ENST00000672743.1:n.150C>A
ENST00000673284.1:c.1138C>A ENSP00000499852.1:p.His380Asn
ENST00000336642.8:c.190C>A ENSP00000338009.4:p.His64Asn
ENST00000345378.6:c.1141C>A ENSP00000223366.2:p.His381Asn
ENST00000395796.7:c.1135C>A ENSP00000379142.3:p.His379Asn
ENST00000403799.7:c.1138C>A ENSP00000384247.3:p.His380Asn
ENST00000437084.1:c.1087C>A ENSP00000402840.1:p.His363Asn
ENST00000459642.1:n.518C>A
ENST00000616242.4:c.1135C>A ENSP00000482149.1:p.His379Asn
NM_000162.3:c.1138C>A NP_000153.1:p.His380Asn
NM_033507.1:c.1141C>A NP_277042.1:p.His381Asn
NM_033508.1:c.1135C>A NP_277043.1:p.His379Asn
NM_000162.4:c.1138C>A NP_000153.1:p.His380Asn
NM_001354800.1:c.1138C>A NP_001341729.1:p.His380Asn
NM_001354801.1:c.127C>A NP_001341730.1:p.His43Asn
NM_001354802.1:c.-3C>A NP_001341731.1:n.-3C>A
NM_001354803.1:c.172C>A NP_001341732.1:p.His58Asn
NM_033507.2:c.1141C>A NP_277042.1:p.His381Asn
NM_033508.2:c.1135C>A NP_277043.1:p.His379Asn
XM_024446707.1:c.-3C>A XP_024302475.1:n.-3C>A
NM_000162.5:c.1138C>A MANE Select NP_000153.1:p.His380Asn
NM_033507.3:c.1141C>A NP_277042.1:p.His381Asn
NM_033508.3:c.1135C>A NP_277043.1:p.His379Asn
NM_001354803.2:c.172C>A NP_001341732.1:p.His58Asn