Canonical Allele Identifier: CA2695202973
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145489_44145512del , CM000669.2:g.44145489_44145512del GRCh38
NC_000007.13:g.44185088_44185111del , CM000669.1:g.44185088_44185111del GRCh37
NC_000007.12:g.44151613_44151636del NCBI36
NG_008847.1:g.48912_48935del
NG_008847.2:g.57659_57682del

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1236_*1251+8del
ENST00000616242.5:c.*358_*373+8del
ENST00000683378.1:n.464_479+8del
ENST00000336642.9:c.272_287+8del
ENST00000345378.7:c.1241_1256+8del
ENST00000403799.8:c.1238_1253+8del
ENST00000671824.1:c.1301_1316+8del
ENST00000672743.1:n.250_265+8del
ENST00000673284.1:c.1238_1253+8del
ENST00000336642.8:c.290_305+8del
ENST00000345378.6:c.1241_1256+8del
ENST00000395796.7:c.1235_1250+8del
ENST00000403799.7:c.1238_1253+8del
ENST00000437084.1:c.1187_1202+8del
ENST00000459642.1:n.618_633+8del
ENST00000616242.4:c.1235_1250+8del
NM_000162.3:c.1238_1253+8del
NM_033507.1:c.1241_1256+8del
NM_033508.1:c.1235_1250+8del
NM_000162.4:c.1238_1253+8del
NM_001354800.1:c.1238_1253+8del
NM_001354801.1:c.227_242+8del
NM_001354802.1:c.98_113+8del
NM_001354803.1:c.272_287+8del
NM_033507.2:c.1241_1256+8del
NM_033508.2:c.1235_1250+8del
XM_024446707.1:c.98_113+8del
NM_000162.5:c.1238_1253+8del
NM_033507.3:c.1241_1256+8del
NM_033508.3:c.1235_1250+8del
NM_001354803.2:c.272_287+8del