Canonical Allele Identifier: CA1868279124
Gene: ALDOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101425550_101425551delinsCA , CM000671.2:g.101425550_101425551delinsCA GRCh38
NC_000009.11:g.104187832_104187833delinsCA , CM000671.1:g.104187832_104187833delinsCA GRCh37
NC_000009.10:g.103227653_103227654delinsCA NCBI36
NG_012387.1:g.15230_15231delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.701_702delinsTG MANE Select ENSP00000497767.1:p.Val234=
ENST00000648064.1:c.701_702delinsTG ENSP00000497990.1:p.Val234=
ENST00000648758.1:c.701_702delinsTG ENSP00000497731.1:p.Val234=
ENST00000649902.1:c.701_702delinsTG ENSP00000497216.1:p.Val234=
ENST00000374855.8:c.701_702delinsTG ENSP00000363988.4:p.Val234=
ENST00000616752.1:c.701_702delinsTG ENSP00000481363.1:p.Val234=
NM_000035.3:c.701_702delinsTG NP_000026.2:p.Val234=
NM_000035.4:c.701_702delinsTG MANE Select NP_000026.2:p.Val234=
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Search 100 bp 3'