Canonical Allele Identifier: CA1868275577

Gene: ALDOB

Linked Data

• dbSNP Id: rs1831050977

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101421808_101421809insTCAGGTT , CM000671.2:g.101421808_101421809insTCAGGTT	GRCh38
NC_000009.11:g.104184090_104184091insTCAGGTT , CM000671.1:g.104184090_104184091insTCAGGTT	GRCh37
NC_000009.10:g.103223911_103223912insTCAGGTT	NCBI36
NG_012387.1:g.18972_18973insAACCTGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000647789.2:c.1095_*1insAACCTGA MANE Select	ENSP00000497767.1:n.1095_*1insAACCTGA
ENST00000648064.1:c.1095_*1insAACCTGA	ENSP00000497990.1:n.1095_*1insAACCTGA
ENST00000648758.1:c.1095_*1insAACCTGA	ENSP00000497731.1:n.1095_*1insAACCTGA
ENST00000374855.8:c.1095_*1insAACCTGA	ENSP00000363988.4:n.1095_*1insAACCTGA
ENST00000616752.1:c.*107_*108insAACCTGA	ENSP00000481363.1:n.*107_*108insAACCTGA
NM_000035.3:c.1095_*1insAACCTGA	NP_000026.2:n.1095_*1insAACCTGA
NM_000035.4:c.1095_*1insAACCTGA MANE Select	NP_000026.2:n.1095_*1insAACCTGA