Canonical Allele Identifier: CA1868278480
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101424891C= , CM000671.2:g.101424891C= GRCh38
NC_000009.11:g.104187173C= , CM000671.1:g.104187173C= GRCh37
NC_000009.10:g.103226994C= NCBI36
NG_012387.1:g.15890G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.951G= MANE Select ENSP00000497767.1:p.Lys317=
ENST00000648064.1:c.951G= ENSP00000497990.1:p.Lys317=
ENST00000648758.1:c.951G= ENSP00000497731.1:p.Lys317=
ENST00000649902.1:c.951G= ENSP00000497216.1:p.Lys317=
ENST00000374855.8:c.951G= ENSP00000363988.4:p.Lys317=
ENST00000616752.1:c.914G= ENSP00000481363.1:p.Arg305=
NM_000035.3:c.951G= NP_000026.2:p.Lys317=
NM_000035.4:c.951G= MANE Select NP_000026.2:p.Lys317=