Canonical Allele Identifier: CA2578392592

Gene: ALDH7A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.126583005del , CM000667.2:g.126583005del	GRCh38
NC_000005.9:g.125918697del , CM000667.1:g.125918697del	GRCh37
NC_000005.8:g.125946596del	NCBI36
NG_008600.2:g.17390del
NG_008600.3:g.17390del

Transcript Alleles

HGVS	Amino-acid change
ENST00000409134.8:c.394-27del MANE Select	ENSP00000387123.3:n.394-27del
ENST00000412186.2:c.393+931del	ENSP00000414536.2:n.393+931del
ENST00000413020.6:c.394-27del	ENSP00000487936.1:n.394-27del
ENST00000458249.6:c.*303-27del	ENSP00000403929.1:n.*303-27del
ENST00000479989.6:n.577-27del
ENST00000503281.6:c.107-5790del
ENST00000509270.2:c.328-27del	ENSP00000449318.2:n.328-27del
ENST00000509459.6:c.66-5790del
ENST00000511266.6:n.1116-27del
ENST00000635851.1:c.392-27del
ENST00000636062.1:n.289-27del
ENST00000636190.1:n.273-27del
ENST00000636225.1:c.*203-27del	ENSP00000490797.1:n.*203-27del
ENST00000636286.1:n.112-27del
ENST00000636743.1:c.274-27del	ENSP00000489725.1:n.274-27del
ENST00000636808.1:c.*203-27del	ENSP00000490833.1:n.*203-27del
ENST00000636872.1:c.554-27del	ENSP00000490919.1:n.554-27del
ENST00000636879.1:c.394-27del	ENSP00000490811.1:n.394-27del
ENST00000636886.1:c.193-27del	ENSP00000490371.1:n.193-27del
ENST00000637070.1:n.8-27del
ENST00000637206.1:c.394-27del	ENSP00000489895.1:n.394-27del
ENST00000637272.1:c.394-27del	ENSP00000489686.1:n.394-27del
ENST00000637292.1:c.47-27del
ENST00000637782.1:c.394-27del	ENSP00000490024.1:n.394-27del
ENST00000637964.1:c.340-27del	ENSP00000490291.1:n.340-27del
ENST00000638008.1:c.*336-27del	ENSP00000490400.1:n.*336-27del
ENST00000409134.7:c.394-27del	ENSP00000387123.3:n.394-27del
ENST00000413020.5:c.394-27del	ENSP00000487936.1:n.394-27del
ENST00000447989.6:c.475-27del	ENSP00000414132.2:n.475-27del
ENST00000458249.5:c.554-27del	ENSP00000403929.1:n.554-27del
ENST00000503281.5:c.107-5790del
ENST00000509270.1:c.274-27del	ENSP00000449318.1:n.274-27del
ENST00000509459.5:c.66-5790del
ENST00000510111.6:c.307-27del	ENSP00000447388.1:n.307-27del
ENST00000511266.5:n.348+931del
ENST00000553117.5:c.394-27del	ENSP00000448593.1:n.394-27del
NM_001182.4:c.394-27del	NP_001173.2:n.394-27del
NM_001201377.1:c.310-27del	NP_001188306.1:n.310-27del
NM_001202404.1:c.475-27del	NP_001189333.1:n.475-27del
XM_011543417.1:c.-12-27del	XP_011541719.1:n.-12-27del
XM_011543417.2:c.-12-27del	XP_011541719.1:n.-12-27del
NM_001182.5:c.394-27del MANE Select	NP_001173.2:n.394-27del
NM_001201377.2:c.310-27del	NP_001188306.1:n.310-27del
NM_001202404.2:c.394-27del	NP_001189333.2:n.394-27del