Canonical Allele Identifier: CA1580460376
Gene: ALDH7A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.126592690T= , CM000667.2:g.126592690T= GRCh38
NC_000005.9:g.125928382T= , CM000667.1:g.125928382T= GRCh37
NC_000005.8:g.125956281T= NCBI36
NG_008600.2:g.7701A=
NG_008600.3:g.7701A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409134.8:c.286A= MANE Select ENSP00000387123.3:p.Arg96=
ENST00000412186.2:c.286A= ENSP00000414536.2:p.Arg96=
ENST00000413020.6:c.286A= ENSP00000487936.1:p.Arg96=
ENST00000458249.6:c.*195A= ENSP00000403929.1:n.*195A=
ENST00000479989.6:n.469A=
ENST00000503281.6:c.106+2317A=
ENST00000509270.2:c.246+661A= ENSP00000449318.2:n.246+661A=
ENST00000509459.6:c.65+2317A=
ENST00000511266.6:n.1008A=
ENST00000635851.1:c.284A=
ENST00000635858.1:n.125A=
ENST00000635933.1:n.315A=
ENST00000636062.1:n.181A=
ENST00000636190.1:n.165A=
ENST00000636225.1:c.*95A= ENSP00000490797.1:n.*95A=
ENST00000636743.1:c.192+2317A= ENSP00000489725.1:n.192+2317A=
ENST00000636808.1:c.*95A= ENSP00000490833.1:n.*95A=
ENST00000636872.1:c.446A= ENSP00000490919.1:n.446A=
ENST00000636879.1:c.286A= ENSP00000490811.1:p.Arg96=
ENST00000636886.1:c.192+2317A= ENSP00000490371.1:n.192+2317A=
ENST00000637206.1:c.286A= ENSP00000489895.1:p.Arg96=
ENST00000637272.1:c.286A= ENSP00000489686.1:p.Arg96=
ENST00000637782.1:c.286A= ENSP00000490024.1:p.Arg96=
ENST00000637964.1:c.232A= ENSP00000490291.1:p.Arg78=
ENST00000638008.1:c.*95A= ENSP00000490400.1:n.*95A=
ENST00000409134.7:c.286A= ENSP00000387123.3:p.Arg96=
ENST00000412186.1:c.*95A= ENSP00000414536.1:n.*95A=
ENST00000413020.5:c.286A= ENSP00000487936.1:p.Arg96=
ENST00000447989.6:c.367A= ENSP00000414132.2:p.Arg123=
ENST00000458249.5:c.446A= ENSP00000403929.1:n.446A=
ENST00000479989.5:n.469A=
ENST00000503281.5:c.106+2317A=
ENST00000509270.1:c.192+2317A= ENSP00000449318.1:n.192+2317A=
ENST00000509459.5:c.65+2317A=
ENST00000510111.6:c.280A= ENSP00000447388.1:p.Arg94=
ENST00000511266.5:n.241A=
ENST00000553117.5:c.286A= ENSP00000448593.1:p.Arg96=
NM_001182.4:c.286A= NP_001173.2:p.Arg96=
NM_001201377.1:c.202A= NP_001188306.1:p.Arg68=
NM_001202404.1:c.367A= NP_001189333.1:p.Arg123=
XM_011543417.1:c.-120A= XP_011541719.1:n.-120A=
XM_011543417.2:c.-120A= XP_011541719.1:n.-120A=
NM_001182.5:c.286A= MANE Select NP_001173.2:p.Arg96=
NM_001201377.2:c.202A= NP_001188306.1:p.Arg68=
NM_001202404.2:c.286A= NP_001189333.2:p.Arg96=