Canonical Allele Identifier: CA2675067524
Gene: ALDH7A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.126546457T>G , CM000667.2:g.126546457T>G GRCh38
NC_000005.9:g.125882149T>G , CM000667.1:g.125882149T>G GRCh37
NC_000005.8:g.125910048T>G NCBI36
NG_008600.2:g.53934A>C
NG_008600.3:g.53934A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000409134.8:c.1490-58A>C MANE Select ENSP00000387123.3:n.1490-58A>C
ENST00000458249.6:c.*1399-58A>C ENSP00000403929.1:n.*1399-58A>C
ENST00000485852.7:n.237-58A>C
ENST00000497231.7:n.1917-58A>C
ENST00000635851.1:c.1488-58A>C
ENST00000636225.1:c.*1434-58A>C ENSP00000490797.1:n.*1434-58A>C
ENST00000636286.1:n.1255-58A>C
ENST00000636482.1:n.1024-58A>C
ENST00000636743.1:c.1370-58A>C ENSP00000489725.1:n.1370-58A>C
ENST00000636808.1:c.*1299-58A>C ENSP00000490833.1:n.*1299-58A>C
ENST00000636872.1:c.1650-58A>C ENSP00000490919.1:n.1650-58A>C
ENST00000636879.1:c.1535-58A>C ENSP00000490811.1:n.1535-58A>C
ENST00000636886.1:c.1289-58A>C ENSP00000490371.1:n.1289-58A>C
ENST00000637206.1:c.1310-58A>C ENSP00000489895.1:n.1310-58A>C
ENST00000637272.1:c.1481-58A>C ENSP00000489686.1:n.1481-58A>C
ENST00000637292.1:c.946-58A>C
ENST00000637782.1:c.1490-58A>C ENSP00000490024.1:n.1490-58A>C
ENST00000638008.1:c.*1334-58A>C ENSP00000490400.1:n.*1334-58A>C
ENST00000638010.1:n.1436-58A>C
ENST00000409134.7:c.1490-58A>C ENSP00000387123.3:n.1490-58A>C
ENST00000447989.6:c.1379-58A>C ENSP00000414132.2:n.1379-58A>C
ENST00000485852.6:n.237-58A>C
ENST00000497231.6:n.1700-58A>C
ENST00000553117.5:c.1298-58A>C ENSP00000448593.1:n.1298-58A>C
NM_001182.4:c.1490-58A>C NP_001173.2:n.1490-58A>C
NM_001201377.1:c.1406-58A>C NP_001188306.1:n.1406-58A>C
NM_001202404.1:c.1379-58A>C NP_001189333.1:n.1379-58A>C
XM_011543417.1:c.1085-58A>C XP_011541719.1:n.1085-58A>C
XM_011543417.2:c.1085-58A>C XP_011541719.1:n.1085-58A>C
NM_001182.5:c.1490-58A>C MANE Select NP_001173.2:n.1490-58A>C
NM_001201377.2:c.1406-58A>C NP_001188306.1:n.1406-58A>C
NM_001202404.2:c.1298-58A>C NP_001189333.2:n.1298-58A>C