Canonical Allele Identifier: CA289417

Gene: ALDH7A1

Linked Data

• ClinVar Variation Id: 136377
• ClinVar RCV Id: RCV002055409
• dbSNP Id: rs17597559
• ExAC: 5:125887693 C / T
• gnomAD v2: 5-125887693-C-T
• gnomAD v3: 5-126552001-C-T
• gnomAD v4: 5-126552001-C-T
• MyVariant Identifiers: chr5:g.125887693C>T (hg19) ; chr5:g.126552001C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.126552001C>T , CM000667.2:g.126552001C>T	GRCh38
NC_000005.9:g.125887693C>T , CM000667.1:g.125887693C>T	GRCh37
NC_000005.8:g.125915592C>T	NCBI36
NG_008600.2:g.48390G>A
NG_008600.3:g.48390G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000409134.8:c.1317+20G>A MANE Select	ENSP00000387123.3:n.1317+20G>A
ENST00000458249.6:c.*1226+20G>A	ENSP00000403929.1:n.*1226+20G>A
ENST00000497231.7:n.1744+20G>A
ENST00000503281.6:c.906+20G>A
ENST00000635851.1:c.1315+20G>A
ENST00000636062.1:n.1212+20G>A
ENST00000636225.1:c.*1261+20G>A	ENSP00000490797.1:n.*1261+20G>A
ENST00000636286.1:n.1035+20G>A
ENST00000636482.1:n.804+20G>A
ENST00000636743.1:c.1197+20G>A	ENSP00000489725.1:n.1197+20G>A
ENST00000636808.1:c.*1126+20G>A	ENSP00000490833.1:n.*1126+20G>A
ENST00000636872.1:c.1477+20G>A	ENSP00000490919.1:n.1477+20G>A
ENST00000636879.1:c.1362+20G>A	ENSP00000490811.1:n.1362+20G>A
ENST00000636886.1:c.1116+20G>A	ENSP00000490371.1:n.1116+20G>A
ENST00000637206.1:c.1137+20G>A	ENSP00000489895.1:n.1137+20G>A
ENST00000637272.1:c.1308+20G>A	ENSP00000489686.1:n.1308+20G>A
ENST00000637292.1:c.774-1708G>A
ENST00000637782.1:c.1317+20G>A	ENSP00000490024.1:n.1317+20G>A
ENST00000638008.1:c.*1161+20G>A	ENSP00000490400.1:n.*1161+20G>A
ENST00000638010.1:n.1263+20G>A
ENST00000409134.7:c.1317+20G>A	ENSP00000387123.3:n.1317+20G>A
ENST00000447989.6:c.1206+20G>A	ENSP00000414132.2:n.1206+20G>A
ENST00000476328.1:n.82+20G>A
ENST00000497231.6:n.1527+20G>A
ENST00000553117.5:c.1125+20G>A	ENSP00000448593.1:n.1125+20G>A
NM_001182.4:c.1317+20G>A	NP_001173.2:n.1317+20G>A
NM_001201377.1:c.1233+20G>A	NP_001188306.1:n.1233+20G>A
NM_001202404.1:c.1206+20G>A	NP_001189333.1:n.1206+20G>A
XM_011543417.1:c.912+20G>A	XP_011541719.1:n.912+20G>A
XM_011543417.2:c.912+20G>A	XP_011541719.1:n.912+20G>A
NM_001182.5:c.1317+20G>A MANE Select	NP_001173.2:n.1317+20G>A
NM_001201377.2:c.1233+20G>A	NP_001188306.1:n.1233+20G>A
NM_001202404.2:c.1125+20G>A	NP_001189333.2:n.1125+20G>A