Canonical Allele Identifier: CA1703635883
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44149831A= , CM000669.2:g.44149831A= GRCh38
NC_000007.13:g.44189430A= , CM000669.1:g.44189430A= GRCh37
NC_000007.12:g.44155955A= NCBI36
NG_008847.1:g.44593T=
NG_008847.2:g.53340T=

Transcript Alleles

HGVS Amino-acid change
ENST00000395796.8:c.*606T= ENSP00000379142.4:n.*606T=
ENST00000616242.5:c.608T= ENSP00000482149.2:p.Val203=
ENST00000682635.1:n.1094T=
ENST00000345378.7:c.611T= ENSP00000223366.2:p.Val204=
ENST00000403799.8:c.608T= MANE Select ENSP00000384247.3:p.Val203=
ENST00000671824.1:c.608T= ENSP00000500264.1:p.Val203=
ENST00000673284.1:c.608T= ENSP00000499852.1:p.Val203=
ENST00000345378.6:c.611T= ENSP00000223366.2:p.Val204=
ENST00000395796.7:c.605T= ENSP00000379142.3:p.Val202=
ENST00000403799.7:c.608T= ENSP00000384247.3:p.Val203=
ENST00000437084.1:c.557T= ENSP00000402840.1:p.Val186=
ENST00000616242.4:n.605T= ENSP00000482149.1:p.Val202=
NM_000162.3:c.608T= NP_000153.1:p.Val203=
NM_033507.1:c.611T= NP_277042.1:p.Val204=
NM_033508.1:c.605T= NP_277043.1:p.Val202=
NM_000162.4:c.608T= NP_000153.1:p.Val203=
NM_001354800.1:c.608T= NP_001341729.1:p.Val203=
NM_033507.2:c.611T= NP_277042.1:p.Val204=
NM_033508.2:c.605T= NP_277043.1:p.Val202=
NM_000162.5:c.608T= MANE Select NP_000153.1:p.Val203=
NM_033507.3:c.611T= NP_277042.1:p.Val204=
NM_033508.3:c.605T= NP_277043.1:p.Val202=