Canonical Allele Identifier: CA645547393
Gene: ALDOB HGNC NCBI

Linked Data

COSMIC: COSM372053
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101427578_101427579delinsTT , CM000671.2:g.101427578_101427579delinsTT GRCh38
NC_000009.11:g.104189860_104189861delinsTT , CM000671.1:g.104189860_104189861delinsTT GRCh37
NC_000009.10:g.103229681_103229682delinsTT NCBI36
NG_012387.1:g.13202_13203delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.443_444delinsAA MANE Select ENSP00000497767.1:p.Trp148Ter
ENST00000648064.1:c.443_444delinsAA ENSP00000497990.1:p.Trp148Ter
ENST00000648758.1:c.443_444delinsAA ENSP00000497731.1:p.Trp148Ter
ENST00000649902.1:c.443_444delinsAA ENSP00000497216.1:p.Trp148Ter
ENST00000374855.8:c.443_444delinsAA ENSP00000363988.4:p.Trp148Ter
ENST00000468981.3:n.68-941_68-940delinsAA
ENST00000616752.1:c.443_444delinsAA ENSP00000481363.1:p.Trp148Ter
NM_000035.3:c.443_444delinsAA NP_000026.2:p.Trp148Ter
NM_000035.4:c.443_444delinsAA MANE Select NP_000026.2:p.Trp148Ter
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