Canonical Allele Identifier: CA1868281297

Gene: ALDOB

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101430109_101430111delinsTTG , CM000671.2:g.101430109_101430111delinsTTG	GRCh38
NC_000009.11:g.104192391_104192393delinsTTG , CM000671.1:g.104192391_104192393delinsTTG	GRCh37
NC_000009.10:g.103232212_103232214delinsTTG	NCBI36
NG_012387.1:g.10670_10672delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.113-145_113-143delinsCAA MANE Select	ENSP00000497767.1:n.113-145_113-143delinsCAA
ENST00000648064.1:c.113-145_113-143delinsCAA	ENSP00000497990.1:n.113-145_113-143delinsCAA
ENST00000648423.1:c.113-145_113-143delinsCAA	ENSP00000497985.1:n.113-145_113-143delinsCAA
ENST00000648758.1:c.113-145_113-143delinsCAA	ENSP00000497731.1:n.113-145_113-143delinsCAA
ENST00000648906.1:n.283-145_283-143delinsCAA
ENST00000649902.1:c.113-145_113-143delinsCAA	ENSP00000497216.1:n.113-145_113-143delinsCAA
ENST00000650613.1:n.189-145_189-143delinsCAA
ENST00000374855.8:c.113-145_113-143delinsCAA	ENSP00000363988.4:n.113-145_113-143delinsCAA
ENST00000616752.1:c.113-145_113-143delinsCAA	ENSP00000481363.1:n.113-145_113-143delinsCAA
NM_000035.3:c.113-145_113-143delinsCAA	NP_000026.2:n.113-145_113-143delinsCAA
NM_000035.4:c.113-145_113-143delinsCAA MANE Select	NP_000026.2:n.113-145_113-143delinsCAA