Canonical Allele Identifier: CA857730812

Gene: ALDOB

Linked Data

• dbSNP Id: rs1307879295
• MyVariant Identifiers: chr9:g.104187450_104187458del (hg19) ; chr9:g.101425168_101425176del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101425170_101425178del , CM000671.2:g.101425170_101425178del	GRCh38
NC_000009.11:g.104187452_104187460del , CM000671.1:g.104187452_104187460del	GRCh37
NC_000009.10:g.103227273_103227281del	NCBI36
NG_012387.1:g.15605_15613del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.800-134_800-126del MANE Select	ENSP00000497767.1:n.800-134_800-126del
ENST00000648064.1:c.800-134_800-126del	ENSP00000497990.1:n.800-134_800-126del
ENST00000648758.1:c.800-134_800-126del	ENSP00000497731.1:n.800-134_800-126del
ENST00000649902.1:c.800-134_800-126del	ENSP00000497216.1:n.800-134_800-126del
ENST00000374855.8:c.800-134_800-126del	ENSP00000363988.4:n.800-134_800-126del
ENST00000616752.1:c.800-134_800-126del	ENSP00000481363.1:n.800-134_800-126del
NM_000035.3:c.800-134_800-126del	NP_000026.2:n.800-134_800-126del
NM_000035.4:c.800-134_800-126del MANE Select	NP_000026.2:n.800-134_800-126del