Canonical Allele Identifier: CA2695203142

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44149937_44149969del , CM000669.2:g.44149937_44149969del	GRCh38
NC_000007.13:g.44189536_44189568del , CM000669.1:g.44189536_44189568del	GRCh37
NC_000007.12:g.44156061_44156093del	NCBI36
NG_008847.1:g.44456_44488del
NG_008847.2:g.53203_53235del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*577+1_*577+33del
ENST00000616242.5:c.579+1_579+33del
ENST00000682635.1:n.1065+1_1065+33del
ENST00000345378.7:c.582+1_582+33del
ENST00000403799.8:c.579+1_579+33del
ENST00000671824.1:c.579+1_579+33del
ENST00000673284.1:c.579+1_579+33del
ENST00000345378.6:c.582+1_582+33del
ENST00000395796.7:c.576+1_576+33del
ENST00000403799.7:c.579+1_579+33del
ENST00000437084.1:c.528+1_528+33del
ENST00000616242.4:c.576+1_576+33del
NM_000162.3:c.579+1_579+33del
NM_033507.1:c.582+1_582+33del
NM_033508.1:c.576+1_576+33del
NM_000162.4:c.579+1_579+33del
NM_001354800.1:c.579+1_579+33del
NM_033507.2:c.582+1_582+33del
NM_033508.2:c.576+1_576+33del
NM_000162.5:c.579+1_579+33del
NM_033507.3:c.582+1_582+33del
NM_033508.3:c.576+1_576+33del