Canonical Allele Identifier: CA2961187317
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101425644_101425646dup , CM000671.2:g.101425644_101425646dup GRCh38
NC_000009.11:g.104187926_104187928dup , CM000671.1:g.104187926_104187928dup GRCh37
NC_000009.10:g.103227747_103227749dup NCBI36
NG_012387.1:g.15135_15137dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.625-19_625-17dup MANE Select ENSP00000497767.1:n.625-19_625-17dup
ENST00000648064.1:c.625-19_625-17dup ENSP00000497990.1:n.625-19_625-17dup
ENST00000648758.1:c.625-19_625-17dup ENSP00000497731.1:n.625-19_625-17dup
ENST00000649902.1:c.625-19_625-17dup ENSP00000497216.1:n.625-19_625-17dup
ENST00000374855.8:c.625-19_625-17dup ENSP00000363988.4:n.625-19_625-17dup
ENST00000468981.3:n.152-19_152-17dup
ENST00000616752.1:c.625-19_625-17dup ENSP00000481363.1:n.625-19_625-17dup
NM_000035.3:c.625-19_625-17dup NP_000026.2:n.625-19_625-17dup
NM_000035.4:c.625-19_625-17dup MANE Select NP_000026.2:n.625-19_625-17dup