Canonical Allele Identifier: CA2720258646
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs2118345201

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101425462_101425473dup , CM000671.2:g.101425462_101425473dup GRCh38
NC_000009.11:g.104187744_104187755dup , CM000671.1:g.104187744_104187755dup GRCh37
NC_000009.10:g.103227565_103227576dup NCBI36
NG_012387.1:g.15317_15328dup

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.788_799dup MANE Select ENSP00000497767.1:p.Pro266_Gly267insAlaAl...
ENST00000648064.1:c.788_799dup ENSP00000497990.1:p.Pro266_Gly267insAlaAl...
ENST00000648758.1:c.788_799dup ENSP00000497731.1:p.Pro266_Gly267insAlaAl...
ENST00000649902.1:c.788_799dup ENSP00000497216.1:p.Pro266_Gly267insAlaAl...
ENST00000374855.8:c.788_799dup ENSP00000363988.4:p.Pro266_Gly267insAlaAl...
ENST00000616752.1:c.788_799dup ENSP00000481363.1:p.Pro266_Gly267insAlaAl...
NM_000035.3:c.788_799dup NP_000026.2:p.Pro266_Gly267insAlaAlaValPr...
NM_000035.4:c.788_799dup MANE Select NP_000026.2:p.Pro266_Gly267insAlaAlaValPr...