Canonical Allele Identifier: CA2691007030

Gene: ALDOB

Linked Data

• gnomAD v4: 9-101425178-A-ATTTC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101425179_101425180insTTCT , CM000671.2:g.101425179_101425180insTTCT	GRCh38
NC_000009.11:g.104187461_104187462insTTCT , CM000671.1:g.104187461_104187462insTTCT	GRCh37
NC_000009.10:g.103227282_103227283insTTCT	NCBI36
NG_012387.1:g.15602_15603insGAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.800-137_800-136insGAAA MANE Select	ENSP00000497767.1:n.800-137_800-136insGAAA
ENST00000648064.1:c.800-137_800-136insGAAA	ENSP00000497990.1:n.800-137_800-136insGAAA
ENST00000648758.1:c.800-137_800-136insGAAA	ENSP00000497731.1:n.800-137_800-136insGAAA
ENST00000649902.1:c.800-137_800-136insGAAA	ENSP00000497216.1:n.800-137_800-136insGAAA
ENST00000374855.8:c.800-137_800-136insGAAA	ENSP00000363988.4:n.800-137_800-136insGAAA
ENST00000616752.1:c.800-137_800-136insGAAA	ENSP00000481363.1:n.800-137_800-136insGAAA
NM_000035.3:c.800-137_800-136insGAAA	NP_000026.2:n.800-137_800-136insGAAA
NM_000035.4:c.800-137_800-136insGAAA MANE Select	NP_000026.2:n.800-137_800-136insGAAA