Canonical Allele Identifier: CA2691007539
Gene: ALDOB HGNC NCBI

Linked Data

gnomAD v4: 9-101427627-G-GT
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101427627_101427628insT , CM000671.2:g.101427627_101427628insT GRCh38
NC_000009.11:g.104189909_104189910insT , CM000671.1:g.104189909_104189910insT GRCh37
NC_000009.10:g.103229730_103229731insT NCBI36
NG_012387.1:g.13153_13154insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.394_395insA MANE Select ENSP00000497767.1:p.Ser132TyrfsTer13
ENST00000648064.1:c.394_395insA ENSP00000497990.1:p.Ser132TyrfsTer13
ENST00000648758.1:c.394_395insA ENSP00000497731.1:p.Ser132TyrfsTer13
ENST00000649902.1:c.394_395insA ENSP00000497216.1:p.Ser132TyrfsTer13
ENST00000374855.8:c.394_395insA ENSP00000363988.4:p.Ser132TyrfsTer13
ENST00000468981.3:n.68-990_68-989insA
ENST00000616752.1:c.394_395insA ENSP00000481363.1:p.Ser132TyrfsTer13
NM_000035.3:c.394_395insA NP_000026.2:p.Ser132TyrfsTer13
NM_000035.4:c.394_395insA MANE Select NP_000026.2:p.Ser132TyrfsTer13
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Search 100 bp 3'