Canonical Allele Identifier: CA838789086
Gene: GCK HGNC NCBI

Linked Data

dbSNP Id: rs1484275585

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145317_44145323del , CM000669.2:g.44145317_44145323del GRCh38
NC_000007.13:g.44184916_44184922del , CM000669.1:g.44184916_44184922del GRCh37
NC_000007.12:g.44151441_44151447del NCBI36
NG_008847.1:g.49105_49111del
NG_008847.2:g.57852_57858del

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1252-39_*1252-33del ENSP00000379142.4:n.*1252-39_*1252-33del
ENST00000616242.5:c.*374-39_*374-33del ENSP00000482149.2:n.*374-39_*374-33del
ENST00000683378.1:n.480-39_480-33del
ENST00000336642.9:c.288-39_288-33del ENSP00000338009.5:n.288-39_288-33del
ENST00000345378.7:c.1257-39_1257-33del ENSP00000223366.2:n.1257-39_1257-33del
ENST00000403799.8:c.1254-39_1254-33del MANE Select ENSP00000384247.3:n.1254-39_1254-33del
ENST00000671824.1:c.1317-39_1317-33del ENSP00000500264.1:n.1317-39_1317-33del
ENST00000672743.1:n.266-39_266-33del
ENST00000673284.1:c.1254-39_1254-33del ENSP00000499852.1:n.1254-39_1254-33del
ENST00000336642.8:c.306-39_306-33del ENSP00000338009.4:n.306-39_306-33del
ENST00000345378.6:c.1257-39_1257-33del ENSP00000223366.2:n.1257-39_1257-33del
ENST00000395796.7:c.1251-39_1251-33del ENSP00000379142.3:n.1251-39_1251-33del
ENST00000403799.7:c.1254-39_1254-33del ENSP00000384247.3:n.1254-39_1254-33del
ENST00000437084.1:c.1203-39_1203-33del ENSP00000402840.1:n.1203-39_1203-33del
ENST00000459642.1:n.634-39_634-33del
ENST00000616242.4:c.1251-39_1251-33del ENSP00000482149.1:n.1251-39_1251-33del
NM_000162.3:c.1254-39_1254-33del NP_000153.1:n.1254-39_1254-33del
NM_033507.1:c.1257-39_1257-33del NP_277042.1:n.1257-39_1257-33del
NM_033508.1:c.1251-39_1251-33del NP_277043.1:n.1251-39_1251-33del
NM_000162.4:c.1254-39_1254-33del NP_000153.1:n.1254-39_1254-33del
NM_001354800.1:c.1254-39_1254-33del NP_001341729.1:n.1254-39_1254-33del
NM_001354801.1:c.243-39_243-33del NP_001341730.1:n.243-39_243-33del
NM_001354802.1:c.114-39_114-33del NP_001341731.1:n.114-39_114-33del
NM_001354803.1:c.288-39_288-33del NP_001341732.1:n.288-39_288-33del
NM_033507.2:c.1257-39_1257-33del NP_277042.1:n.1257-39_1257-33del
NM_033508.2:c.1251-39_1251-33del NP_277043.1:n.1251-39_1251-33del
XM_024446707.1:c.114-39_114-33del XP_024302475.1:n.114-39_114-33del
NM_000162.5:c.1254-39_1254-33del MANE Select NP_000153.1:n.1254-39_1254-33del
NM_033507.3:c.1257-39_1257-33del NP_277042.1:n.1257-39_1257-33del
NM_033508.3:c.1251-39_1251-33del NP_277043.1:n.1251-39_1251-33del
NM_001354803.2:c.288-39_288-33del NP_001341732.1:n.288-39_288-33del