Canonical Allele Identifier: CA1580440346
Gene: ALDH7A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.126544862T= , CM000667.2:g.126544862T= GRCh38
NC_000005.9:g.125880554T= , CM000667.1:g.125880554T= GRCh37
NC_000005.8:g.125908453T= NCBI36
NG_008600.2:g.55529A=
NG_008600.3:g.55529A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409134.8:c.*103A= MANE Select ENSP00000387123.3:n.*103A=
ENST00000458249.6:c.*1632A= ENSP00000403929.1:n.*1632A=
ENST00000485852.7:n.470A=
ENST00000497231.7:n.2150A=
ENST00000635851.1:c.1563+1462A=
ENST00000636482.1:n.1257A=
ENST00000636743.1:c.*103A= ENSP00000489725.1:n.*103A=
ENST00000636808.1:c.*1532A= ENSP00000490833.1:n.*1532A=
ENST00000636872.1:c.1883A= ENSP00000490919.1:n.1883A=
ENST00000636879.1:c.*103A= ENSP00000490811.1:n.*103A=
ENST00000636886.1:c.*103A= ENSP00000490371.1:n.*103A=
ENST00000637206.1:c.*103A= ENSP00000489895.1:n.*103A=
ENST00000637272.1:c.*103A= ENSP00000489686.1:n.*103A=
ENST00000637292.1:c.1179A=
ENST00000637782.1:c.1565+1462A= ENSP00000490024.1:n.1565+1462A=
ENST00000638008.1:c.*1567A= ENSP00000490400.1:n.*1567A=
ENST00000638010.1:n.1669A=
ENST00000409134.7:c.*103A= ENSP00000387123.3:n.*103A=
ENST00000447989.6:c.*103A= ENSP00000414132.2:n.*103A=
ENST00000485852.6:n.470A=
ENST00000497231.6:n.1933A=
ENST00000553117.5:c.*103A= ENSP00000448593.1:n.*103A=
NM_001182.4:c.*103A= NP_001173.2:n.*103A=
NM_001201377.1:c.*103A= NP_001188306.1:n.*103A=
NM_001202404.1:c.*103A= NP_001189333.1:n.*103A=
XM_011543417.1:c.*103A= XP_011541719.1:n.*103A=
XM_011543417.2:c.*103A= XP_011541719.1:n.*103A=
NM_001182.5:c.*103A= MANE Select NP_001173.2:n.*103A=
NM_001201377.2:c.*103A= NP_001188306.1:n.*103A=
NM_001202404.2:c.*103A= NP_001189333.2:n.*103A=