Canonical Allele Identifier: CA1081237064
Gene: ALDH7A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.126577016_126577017insGA , CM000667.2:g.126577016_126577017insGA GRCh38
NC_000005.9:g.125912708_125912709insGA , CM000667.1:g.125912708_125912709insGA GRCh37
NC_000005.8:g.125940607_125940608insGA NCBI36
NG_008600.2:g.23374_23375insTC
NG_008600.3:g.23374_23375insTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000409134.8:c.650+62_650+63insTC MANE Select ENSP00000387123.3:n.650+62_650+63insTC
ENST00000412186.2:c.526+62_526+63insTC ENSP00000414536.2:n.526+62_526+63insTC
ENST00000413020.6:c.650+62_650+63insTC ENSP00000487936.1:n.650+62_650+63insTC
ENST00000458249.6:c.*559+62_*559+63insTC ENSP00000403929.1:n.*559+62_*559+63insTC
ENST00000503281.6:c.239+62_239+63insTC
ENST00000509459.6:c.198+62_198+63insTC
ENST00000511266.6:n.1372+62_1372+63insTC
ENST00000635851.1:c.648+62_648+63insTC
ENST00000636062.1:n.545+62_545+63insTC
ENST00000636225.1:c.*459+62_*459+63insTC ENSP00000490797.1:n.*459+62_*459+63insTC
ENST00000636286.1:n.368+62_368+63insTC
ENST00000636743.1:c.530+62_530+63insTC ENSP00000489725.1:n.530+62_530+63insTC
ENST00000636808.1:c.*459+62_*459+63insTC ENSP00000490833.1:n.*459+62_*459+63insTC
ENST00000636872.1:c.810+62_810+63insTC ENSP00000490919.1:n.810+62_810+63insTC
ENST00000636879.1:c.695+62_695+63insTC ENSP00000490811.1:n.695+62_695+63insTC
ENST00000636886.1:c.449+62_449+63insTC ENSP00000490371.1:n.449+62_449+63insTC
ENST00000637206.1:c.650+62_650+63insTC ENSP00000489895.1:n.650+62_650+63insTC
ENST00000637272.1:c.650+62_650+63insTC ENSP00000489686.1:n.650+62_650+63insTC
ENST00000637292.1:c.303+62_303+63insTC
ENST00000637782.1:c.650+62_650+63insTC ENSP00000490024.1:n.650+62_650+63insTC
ENST00000637964.1:c.596+62_596+63insTC ENSP00000490291.1:n.596+62_596+63insTC
ENST00000638008.1:c.*592+62_*592+63insTC ENSP00000490400.1:n.*592+62_*592+63insTC
ENST00000409134.7:c.650+62_650+63insTC ENSP00000387123.3:n.650+62_650+63insTC
ENST00000413020.5:c.650+62_650+63insTC ENSP00000487936.1:n.650+62_650+63insTC
ENST00000433026.5:n.177+62_177+63insTC
ENST00000447989.6:c.731+62_731+63insTC ENSP00000414132.2:n.731+62_731+63insTC
ENST00000458249.5:c.810+62_810+63insTC ENSP00000403929.1:n.810+62_810+63insTC
ENST00000503281.5:c.239+62_239+63insTC
ENST00000509459.5:c.198+62_198+63insTC
ENST00000510111.6:c.563+62_563+63insTC ENSP00000447388.1:n.563+62_563+63insTC
ENST00000511266.5:n.481+62_481+63insTC
ENST00000553117.5:c.650+62_650+63insTC ENSP00000448593.1:n.650+62_650+63insTC
NM_001182.4:c.650+62_650+63insTC NP_001173.2:n.650+62_650+63insTC
NM_001201377.1:c.566+62_566+63insTC NP_001188306.1:n.566+62_566+63insTC
NM_001202404.1:c.731+62_731+63insTC NP_001189333.1:n.731+62_731+63insTC
XM_011543417.1:c.245+62_245+63insTC XP_011541719.1:n.245+62_245+63insTC
XM_011543417.2:c.245+62_245+63insTC XP_011541719.1:n.245+62_245+63insTC
NM_001182.5:c.650+62_650+63insTC MANE Select NP_001173.2:n.650+62_650+63insTC
NM_001201377.2:c.566+62_566+63insTC NP_001188306.1:n.566+62_566+63insTC
NM_001202404.2:c.650+62_650+63insTC NP_001189333.2:n.650+62_650+63insTC