Canonical Allele Identifier: CA1868281536

Gene: ALDOB

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101430611_101430612delinsCT , CM000671.2:g.101430611_101430612delinsCT	GRCh38
NC_000009.11:g.104192893_104192894delinsCT , CM000671.1:g.104192893_104192894delinsCT	GRCh37
NC_000009.10:g.103232714_103232715delinsCT	NCBI36
NG_012387.1:g.10169_10170delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000647789.2:c.112+164_112+165delinsAG MANE Select	ENSP00000497767.1:n.112+164_112+165delinsAG
ENST00000648064.1:c.112+164_112+165delinsAG	ENSP00000497990.1:n.112+164_112+165delinsAG
ENST00000648423.1:c.112+164_112+165delinsAG	ENSP00000497985.1:n.112+164_112+165delinsAG
ENST00000648758.1:c.112+164_112+165delinsAG	ENSP00000497731.1:n.112+164_112+165delinsAG
ENST00000648906.1:n.282+164_282+165delinsAG
ENST00000649902.1:c.112+164_112+165delinsAG	ENSP00000497216.1:n.112+164_112+165delinsAG
ENST00000650613.1:n.188+164_188+165delinsAG
ENST00000374855.8:c.112+164_112+165delinsAG	ENSP00000363988.4:n.112+164_112+165delinsAG
ENST00000616752.1:c.112+164_112+165delinsAG	ENSP00000481363.1:n.112+164_112+165delinsAG
NM_000035.3:c.112+164_112+165delinsAG	NP_000026.2:n.112+164_112+165delinsAG
NM_000035.4:c.112+164_112+165delinsAG MANE Select	NP_000026.2:n.112+164_112+165delinsAG