Canonical Allele Identifier: CA374265719

Gene: ALDOB

Linked Data

• MyVariant Identifiers: chr9:g.104192083A>G (hg19) ; chr9:g.101429801A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101429801A>G , CM000671.2:g.101429801A>G	GRCh38
NC_000009.11:g.104192083A>G , CM000671.1:g.104192083A>G	GRCh37
NC_000009.10:g.103231904A>G	NCBI36
NG_012387.1:g.10980T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.278T>C MANE Select	ENSP00000497767.1:p.Leu93Pro
ENST00000648064.1:c.278T>C	ENSP00000497990.1:p.Leu93Pro
ENST00000648758.1:c.278T>C	ENSP00000497731.1:p.Leu93Pro
ENST00000648906.1:n.448T>C
ENST00000649902.1:c.278T>C	ENSP00000497216.1:p.Leu93Pro
ENST00000650613.1:n.354T>C
ENST00000374855.8:c.278T>C	ENSP00000363988.4:p.Leu93Pro
ENST00000468981.3:n.67+8T>C
ENST00000616752.1:c.278T>C	ENSP00000481363.1:p.Leu93Pro
NM_000035.3:c.278T>C	NP_000026.2:p.Leu93Pro
NM_000035.4:c.278T>C MANE Select	NP_000026.2:p.Leu93Pro