Canonical Allele Identifier: CA1868278365

Gene: ALDOB

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101424818_101424820delinsTAG , CM000671.2:g.101424818_101424820delinsTAG	GRCh38
NC_000009.11:g.104187100_104187102delinsTAG , CM000671.1:g.104187100_104187102delinsTAG	GRCh37
NC_000009.10:g.103226921_103226923delinsTAG	NCBI36
NG_012387.1:g.15961_15963delinsCTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000647789.2:c.999+23_999+25delinsCTA MANE Select	ENSP00000497767.1:n.999+23_999+25delinsCTA
ENST00000648064.1:c.999+23_999+25delinsCTA	ENSP00000497990.1:n.999+23_999+25delinsCTA
ENST00000648758.1:c.999+23_999+25delinsCTA	ENSP00000497731.1:n.999+23_999+25delinsCTA
ENST00000649902.1:c.1022_1024delinsCTA	ENSP00000497216.1:p.Ser341=
ENST00000374855.8:c.999+23_999+25delinsCTA	ENSP00000363988.4:n.999+23_999+25delinsCTA
ENST00000616752.1:c.*11+23_*11+25delinsCTA	ENSP00000481363.1:n.*11+23_*11+25delinsCTA
NM_000035.3:c.999+23_999+25delinsCTA	NP_000026.2:n.999+23_999+25delinsCTA
NM_000035.4:c.999+23_999+25delinsCTA MANE Select	NP_000026.2:n.999+23_999+25delinsCTA