Canonical Allele Identifier: CA2340417865
Gene: ALDH16A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49465749C= , CM000681.2:g.49465749C= GRCh38
NC_000019.9:g.49969006C= , CM000681.1:g.49969006C= GRCh37
NC_000019.8:g.54660818C= NCBI36
NG_012747.1:g.17534C=

Transcript Alleles

HGVS Amino-acid Change
NM_153329.4:c.1580C= MANE Select NP_699160.2:p.Pro527=
ENST00000293350.9:c.1580C= MANE Select ENSP00000293350.3:p.Pro527=
NM_001145396.1:c.1427C= NP_001138868.1:p.Pro476=
NM_001145396.2:c.1427C= NP_001138868.1:p.Pro476=
NM_153329.3:c.1580C= NP_699160.2:p.Pro527=
ENST00000293350.8:c.1580C= ENSP00000293350.3:p.Pro527=
ENST00000455361.6:c.1427C= ENSP00000410142.1:p.Pro476=
ENST00000540132.5:c.1091C= ENSP00000445088.1:p.Pro364=
ENST00000593417.5:c.*1038C= ENSP00000470160.1:n.*1038C=
ENST00000599536.1:c.337+987C=
ENST00000599652.5:n.1758-32C=
ENST00000600265.1:c.227C= ENSP00000469507.1:p.Pro76=
XM_011526441.1:c.1493C= XP_011524743.1:p.Pro498=
XM_011526442.1:c.1493C= XP_011524744.1:p.Pro498=