Canonical Allele Identifier: CA1868280559

Gene: ALDOB

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101428582_101428586delinsGAACT , CM000671.2:g.101428582_101428586delinsGAACT	GRCh38
NC_000009.11:g.104190864_104190868delinsGAACT , CM000671.1:g.104190864_104190868delinsGAACT	GRCh37
NC_000009.10:g.103230685_103230689delinsGAACT	NCBI36
NG_012387.1:g.12195_12199delinsAGTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.325-63_325-59delinsAGTTC MANE Select	ENSP00000497767.1:n.325-63_325-59delinsAGTTC
ENST00000648064.1:c.325-63_325-59delinsAGTTC	ENSP00000497990.1:n.325-63_325-59delinsAGTTC
ENST00000648758.1:c.325-63_325-59delinsAGTTC	ENSP00000497731.1:n.325-63_325-59delinsAGTTC
ENST00000649902.1:c.325-63_325-59delinsAGTTC	ENSP00000497216.1:n.325-63_325-59delinsAGTTC
ENST00000374855.8:c.325-63_325-59delinsAGTTC	ENSP00000363988.4:n.325-63_325-59delinsAGTTC
ENST00000468981.3:n.67+1223_67+1227delinsAGTTC
ENST00000616752.1:c.325-63_325-59delinsAGTTC	ENSP00000481363.1:n.325-63_325-59delinsAGTTC
NM_000035.3:c.325-63_325-59delinsAGTTC	NP_000026.2:n.325-63_325-59delinsAGTTC
NM_000035.4:c.325-63_325-59delinsAGTTC MANE Select	NP_000026.2:n.325-63_325-59delinsAGTTC