Canonical Allele Identifier: CA1703612889
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145584A= , CM000669.2:g.44145584A= GRCh38
NC_000007.13:g.44185183A= , CM000669.1:g.44185183A= GRCh37
NC_000007.12:g.44151708A= NCBI36
NG_008847.1:g.48840T=
NG_008847.2:g.57587T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1164T= ENSP00000379142.4:n.*1164T=
ENST00000616242.5:c.*286T= ENSP00000482149.2:n.*286T=
ENST00000683378.1:n.392T=
ENST00000336642.9:c.200T= ENSP00000338009.5:p.Val67=
ENST00000345378.7:c.1169T= ENSP00000223366.2:p.Val390=
ENST00000403799.8:c.1166T= MANE Select ENSP00000384247.3:p.Val389=
ENST00000671824.1:c.1229T= ENSP00000500264.1:p.Val410=
ENST00000672743.1:n.178T=
ENST00000673284.1:c.1166T= ENSP00000499852.1:p.Val389=
ENST00000336642.8:c.218T= ENSP00000338009.4:p.Val73=
ENST00000345378.6:c.1169T= ENSP00000223366.2:p.Val390=
ENST00000395796.7:c.1163T= ENSP00000379142.3:p.Val388=
ENST00000403799.7:c.1166T= ENSP00000384247.3:p.Val389=
ENST00000437084.1:c.1115T= ENSP00000402840.1:p.Val372=
ENST00000459642.1:n.546T=
ENST00000616242.4:c.1163T= ENSP00000482149.1:p.Val388=
NM_000162.3:c.1166T= NP_000153.1:p.Val389=
NM_033507.1:c.1169T= NP_277042.1:p.Val390=
NM_033508.1:c.1163T= NP_277043.1:p.Val388=
NM_000162.4:c.1166T= NP_000153.1:p.Val389=
NM_001354800.1:c.1166T= NP_001341729.1:p.Val389=
NM_001354801.1:c.155T= NP_001341730.1:p.Val52=
NM_001354802.1:c.26T= NP_001341731.1:p.Val9=
NM_001354803.1:c.200T= NP_001341732.1:p.Val67=
NM_033507.2:c.1169T= NP_277042.1:p.Val390=
NM_033508.2:c.1163T= NP_277043.1:p.Val388=
XM_024446707.1:c.26T= XP_024302475.1:p.Val9=
NM_000162.5:c.1166T= MANE Select NP_000153.1:p.Val389=
NM_033507.3:c.1169T= NP_277042.1:p.Val390=
NM_033508.3:c.1163T= NP_277043.1:p.Val388=
NM_001354803.2:c.200T= NP_001341732.1:p.Val67=