Canonical Allele Identifier: CA446280125

Gene: ALDH7A1

Linked Data

• MyVariant Identifiers: chr5:g.125880683G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.126544991G>A , CM000667.2:g.126544991G>A	GRCh38
NC_000005.9:g.125880683G>A , CM000667.1:g.125880683G>A	GRCh37
NC_000005.8:g.125908582G>A	NCBI36
NG_008600.2:g.55400C>T
NG_008600.3:g.55400C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409134.8:c.1594C>T MANE Select	ENSP00000387123.3:p.Leu532=
ENST00000458249.6:c.*1503C>T	ENSP00000403929.1:n.*1503C>T
ENST00000485852.7:n.341C>T
ENST00000497231.7:n.2021C>T
ENST00000635851.1:c.1563+1333C>T
ENST00000636286.1:n.1359C>T
ENST00000636482.1:n.1128C>T
ENST00000636743.1:c.1474C>T	ENSP00000489725.1:p.Leu492=
ENST00000636808.1:c.*1403C>T	ENSP00000490833.1:n.*1403C>T
ENST00000636872.1:c.1754C>T	ENSP00000490919.1:n.1754C>T
ENST00000636879.1:c.1639C>T	ENSP00000490811.1:p.Leu547=
ENST00000636886.1:c.1393C>T	ENSP00000490371.1:p.Leu465=
ENST00000637206.1:c.1414C>T	ENSP00000489895.1:p.Leu472=
ENST00000637272.1:c.1585C>T	ENSP00000489686.1:p.Leu529=
ENST00000637292.1:c.1050C>T
ENST00000637782.1:c.1565+1333C>T	ENSP00000490024.1:n.1565+1333C>T
ENST00000638008.1:c.*1438C>T	ENSP00000490400.1:n.*1438C>T
ENST00000638010.1:n.1540C>T
ENST00000409134.7:c.1594C>T	ENSP00000387123.3:p.Leu532=
ENST00000447989.6:c.1483C>T	ENSP00000414132.2:p.Leu495=
ENST00000485852.6:n.341C>T
ENST00000497231.6:n.1804C>T
ENST00000553117.5:c.1402C>T	ENSP00000448593.1:p.Leu468=
NM_001182.4:c.1594C>T	NP_001173.2:p.Leu532=
NM_001201377.1:c.1510C>T	NP_001188306.1:p.Leu504=
NM_001202404.1:c.1483C>T	NP_001189333.1:p.Leu495=
XM_011543417.1:c.1189C>T	XP_011541719.1:p.Leu397=
XM_011543417.2:c.1189C>T	XP_011541719.1:p.Leu397=
NM_001182.5:c.1594C>T MANE Select	NP_001173.2:p.Leu532=
NM_001201377.2:c.1510C>T	NP_001188306.1:p.Leu504=
NM_001202404.2:c.1402C>T	NP_001189333.2:p.Leu468=