Canonical Allele Identifier: CA1703635842
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44149747A= , CM000669.2:g.44149747A= GRCh38
NC_000007.13:g.44189346A= , CM000669.1:g.44189346A= GRCh37
NC_000007.12:g.44155871A= NCBI36
NG_008847.1:g.44677T=
NG_008847.2:g.53424T=

Transcript Alleles

HGVS Amino-acid change
ENST00000395796.8:c.*677+13T= ENSP00000379142.4:n.*677+13T=
ENST00000616242.5:c.679+13T= ENSP00000482149.2:n.679+13T=
ENST00000682635.1:n.1178T=
ENST00000345378.7:c.682+13T= ENSP00000223366.2:n.682+13T=
ENST00000403799.8:c.679+13T= MANE Select ENSP00000384247.3:n.679+13T=
ENST00000671824.1:c.679+13T= ENSP00000500264.1:n.679+13T=
ENST00000673284.1:c.679+13T= ENSP00000499852.1:n.679+13T=
ENST00000345378.6:c.682+13T= ENSP00000223366.2:n.682+13T=
ENST00000395796.7:c.676+13T= ENSP00000379142.3:n.676+13T=
ENST00000403799.7:c.679+13T= ENSP00000384247.3:n.679+13T=
ENST00000437084.1:c.628+13T= ENSP00000402840.1:n.628+13T=
ENST00000616242.4:n.676+13T= ENSP00000482149.1:n.676+13T=
NM_000162.3:c.679+13T= NP_000153.1:n.679+13T=
NM_033507.1:c.682+13T= NP_277042.1:n.682+13T=
NM_033508.1:c.676+13T= NP_277043.1:n.676+13T=
XR_927223.1:n.262A=
NM_000162.4:c.679+13T= NP_000153.1:n.679+13T=
NM_001354800.1:c.679+13T= NP_001341729.1:n.679+13T=
NM_033507.2:c.682+13T= NP_277042.1:n.682+13T=
NM_033508.2:c.676+13T= NP_277043.1:n.676+13T=
XR_927223.2:n.262A=
NM_000162.5:c.679+13T= MANE Select NP_000153.1:n.679+13T=
NM_033507.3:c.682+13T= NP_277042.1:n.682+13T=
NM_033508.3:c.676+13T= NP_277043.1:n.676+13T=