Canonical Allele Identifier: CA918520753
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs1588169057

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421907_101421908insAAAGCCTCCTGGGTTGCCTCCTTGTTT , CM000671.2:g.101421907_101421908insAAAGCCTCCTGGGTTGCCTCCTTGTTT GRCh38
NC_000009.11:g.104184189_104184190insAAAGCCTCCTGGGTTGCCTCCTTGTTT , CM000671.1:g.104184189_104184190insAAAGCCTCCTGGGTTGCCTCCTTGTTT GRCh37
NC_000009.10:g.103224010_103224011insAAAGCCTCCTGGGTTGCCTCCTTGTTT NCBI36
NG_012387.1:g.18873_18874insAAACAAGGAGGCAACCCAGGAGGCTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.1000-4_1000-3insAAACAAGGAGGCAACCCAGGAGGCTTT MANE Select ENSP00000497767.1:n.1000-4_1000-3insAAACA...
ENST00000648064.1:c.1000-4_1000-3insAAACAAGGAGGCAACCCAGGAGGCTTT ENSP00000497990.1:n.1000-4_1000-3insAAACA...
ENST00000648758.1:c.1000-4_1000-3insAAACAAGGAGGCAACCCAGGAGGCTTT ENSP00000497731.1:n.1000-4_1000-3insAAACA...
ENST00000374855.8:c.1000-4_1000-3insAAACAAGGAGGCAACCCAGGAGGCTTT ENSP00000363988.4:n.1000-4_1000-3insAAACA...
ENST00000616752.1:c.*12-4_*12-3insAAACAAGGAGGCAACCCAGGAGGCTTT ENSP00000481363.1:n.*12-4_*12-3insAAACAAG...
NM_000035.3:c.1000-4_1000-3insAAACAAGGAGGCAACCCAGGAGGCTTT NP_000026.2:n.1000-4_1000-3insAAACAAGGAGG...
NM_000035.4:c.1000-4_1000-3insAAACAAGGAGGCAACCCAGGAGGCTTT MANE Select NP_000026.2:n.1000-4_1000-3insAAACAAGGAGG...