Canonical Allele Identifier: CA374265784

Gene: ALDOB

Linked Data

• MyVariant Identifiers: chr9:g.104192110A>G (hg19) ; chr9:g.101429828A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101429828A>G , CM000671.2:g.101429828A>G	GRCh38
NC_000009.11:g.104192110A>G , CM000671.1:g.104192110A>G	GRCh37
NC_000009.10:g.103231931A>G	NCBI36
NG_012387.1:g.10953T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.251T>C MANE Select	ENSP00000497767.1:p.Leu84Pro
ENST00000648064.1:c.251T>C	ENSP00000497990.1:p.Leu84Pro
ENST00000648758.1:c.251T>C	ENSP00000497731.1:p.Leu84Pro
ENST00000648906.1:n.421T>C
ENST00000649902.1:c.251T>C	ENSP00000497216.1:p.Leu84Pro
ENST00000650613.1:n.327T>C
ENST00000374855.8:c.251T>C	ENSP00000363988.4:p.Leu84Pro
ENST00000468981.3:n.48T>C
ENST00000616752.1:c.251T>C	ENSP00000481363.1:p.Leu84Pro
NM_000035.3:c.251T>C	NP_000026.2:p.Leu84Pro
NM_000035.4:c.251T>C MANE Select	NP_000026.2:p.Leu84Pro