Canonical Allele Identifier: CA2675067931

Gene: ALDH7A1

Linked Data

• gnomAD v4: 5-126552013-ATTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.126552016_126552018del , CM000667.2:g.126552016_126552018del	GRCh38
NC_000005.9:g.125887708_125887710del , CM000667.1:g.125887708_125887710del	GRCh37
NC_000005.8:g.125915607_125915609del	NCBI36
NG_008600.2:g.48375_48377del
NG_008600.3:g.48375_48377del

Transcript Alleles

HGVS	Amino-acid change
ENST00000409134.8:c.1317+5_1317+7del MANE Select	ENSP00000387123.3:n.1317+5_1317+7del
ENST00000458249.6:c.*1226+5_*1226+7del	ENSP00000403929.1:n.*1226+5_*1226+7del
ENST00000497231.7:n.1744+5_1744+7del
ENST00000503281.6:c.906+5_906+7del
ENST00000635851.1:c.1315+5_1315+7del
ENST00000636062.1:n.1212+5_1212+7del
ENST00000636225.1:c.*1261+5_*1261+7del	ENSP00000490797.1:n.*1261+5_*1261+7del
ENST00000636286.1:n.1035+5_1035+7del
ENST00000636482.1:n.804+5_804+7del
ENST00000636743.1:c.1197+5_1197+7del	ENSP00000489725.1:n.1197+5_1197+7del
ENST00000636808.1:c.*1126+5_*1126+7del	ENSP00000490833.1:n.*1126+5_*1126+7del
ENST00000636872.1:c.1477+5_1477+7del	ENSP00000490919.1:n.1477+5_1477+7del
ENST00000636879.1:c.1362+5_1362+7del	ENSP00000490811.1:n.1362+5_1362+7del
ENST00000636886.1:c.1116+5_1116+7del	ENSP00000490371.1:n.1116+5_1116+7del
ENST00000637206.1:c.1137+5_1137+7del	ENSP00000489895.1:n.1137+5_1137+7del
ENST00000637272.1:c.1308+5_1308+7del	ENSP00000489686.1:n.1308+5_1308+7del
ENST00000637292.1:c.774-1723_774-1721del
ENST00000637782.1:c.1317+5_1317+7del	ENSP00000490024.1:n.1317+5_1317+7del
ENST00000638008.1:c.*1161+5_*1161+7del	ENSP00000490400.1:n.*1161+5_*1161+7del
ENST00000638010.1:n.1263+5_1263+7del
ENST00000409134.7:c.1317+5_1317+7del	ENSP00000387123.3:n.1317+5_1317+7del
ENST00000447989.6:c.1206+5_1206+7del	ENSP00000414132.2:n.1206+5_1206+7del
ENST00000476328.1:n.82+5_82+7del
ENST00000497231.6:n.1527+5_1527+7del
ENST00000553117.5:c.1125+5_1125+7del	ENSP00000448593.1:n.1125+5_1125+7del
NM_001182.4:c.1317+5_1317+7del	NP_001173.2:n.1317+5_1317+7del
NM_001201377.1:c.1233+5_1233+7del	NP_001188306.1:n.1233+5_1233+7del
NM_001202404.1:c.1206+5_1206+7del	NP_001189333.1:n.1206+5_1206+7del
XM_011543417.1:c.912+5_912+7del	XP_011541719.1:n.912+5_912+7del
XM_011543417.2:c.912+5_912+7del	XP_011541719.1:n.912+5_912+7del
NM_001182.5:c.1317+5_1317+7del MANE Select	NP_001173.2:n.1317+5_1317+7del
NM_001201377.2:c.1233+5_1233+7del	NP_001188306.1:n.1233+5_1233+7del
NM_001202404.2:c.1125+5_1125+7del	NP_001189333.2:n.1125+5_1125+7del