Canonical Allele Identifier: CA1868280117

Gene: ALDOB

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101427601_101427602delinsCT , CM000671.2:g.101427601_101427602delinsCT	GRCh38
NC_000009.11:g.104189883_104189884delinsCT , CM000671.1:g.104189883_104189884delinsCT	GRCh37
NC_000009.10:g.103229704_103229705delinsCT	NCBI36
NG_012387.1:g.13179_13180delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000647789.2:c.420_421delinsAG MANE Select	ENSP00000497767.1:p.Lys140=
ENST00000648064.1:c.420_421delinsAG	ENSP00000497990.1:p.Lys140=
ENST00000648758.1:c.420_421delinsAG	ENSP00000497731.1:p.Lys140=
ENST00000649902.1:c.420_421delinsAG	ENSP00000497216.1:p.Lys140=
ENST00000374855.8:c.420_421delinsAG	ENSP00000363988.4:p.Lys140=
ENST00000468981.3:n.68-964_68-963delinsAG
ENST00000616752.1:c.420_421delinsAG	ENSP00000481363.1:p.Lys140=
NM_000035.3:c.420_421delinsAG	NP_000026.2:p.Lys140=
NM_000035.4:c.420_421delinsAG MANE Select	NP_000026.2:p.Lys140=