Canonical Allele Identifier: CA2541109412

Gene: ALDH7A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.126544820A>T , CM000667.2:g.126544820A>T	GRCh38
NC_000005.9:g.125880512A>T , CM000667.1:g.125880512A>T	GRCh37
NC_000005.8:g.125908411A>T	NCBI36
NG_008600.2:g.55571T>A
NG_008600.3:g.55571T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409134.8:c.*145T>A MANE Select	ENSP00000387123.3:n.*145T>A
ENST00000458249.6:c.*1674T>A	ENSP00000403929.1:n.*1674T>A
ENST00000485852.7:n.512T>A
ENST00000497231.7:n.2192T>A
ENST00000635851.1:c.1563+1504T>A
ENST00000636482.1:n.1299T>A
ENST00000636743.1:c.*145T>A	ENSP00000489725.1:n.*145T>A
ENST00000636808.1:c.*1574T>A	ENSP00000490833.1:n.*1574T>A
ENST00000636872.1:c.1925T>A	ENSP00000490919.1:n.1925T>A
ENST00000636879.1:c.*145T>A	ENSP00000490811.1:n.*145T>A
ENST00000636886.1:c.*145T>A	ENSP00000490371.1:n.*145T>A
ENST00000637206.1:c.*145T>A	ENSP00000489895.1:n.*145T>A
ENST00000637272.1:c.*145T>A	ENSP00000489686.1:n.*145T>A
ENST00000637292.1:c.1221T>A
ENST00000637782.1:c.1565+1504T>A	ENSP00000490024.1:n.1565+1504T>A
ENST00000638010.1:n.1711T>A
ENST00000409134.7:c.*145T>A	ENSP00000387123.3:n.*145T>A
ENST00000447989.6:c.*145T>A	ENSP00000414132.2:n.*145T>A
ENST00000485852.6:n.512T>A
ENST00000497231.6:n.1975T>A
ENST00000553117.5:c.*145T>A	ENSP00000448593.1:n.*145T>A
NM_001182.4:c.*145T>A	NP_001173.2:n.*145T>A
NM_001201377.1:c.*145T>A	NP_001188306.1:n.*145T>A
NM_001202404.1:c.*145T>A	NP_001189333.1:n.*145T>A
XM_011543417.1:c.*145T>A	XP_011541719.1:n.*145T>A
XM_011543417.2:c.*145T>A	XP_011541719.1:n.*145T>A
NM_001182.5:c.*145T>A MANE Select	NP_001173.2:n.*145T>A
NM_001201377.2:c.*145T>A	NP_001188306.1:n.*145T>A
NM_001202404.2:c.*145T>A	NP_001189333.2:n.*145T>A