Canonical Allele Identifier: CA126924343

Gene: ALDH7A1

Linked Data

• ClinVar Variation Id: 1011813
• ClinVar RCV Id: RCV001309669
• dbSNP Id: rs945175192
• gnomAD v2: 5-125928394-C-G
• gnomAD v3: 5-126592702-C-G
• gnomAD v4: 5-126592702-C-G
• MyVariant Identifiers: chr5:g.125928394C>G (hg19) ; chr5:g.126592702C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.126592702C>G , CM000667.2:g.126592702C>G	GRCh38
NC_000005.9:g.125928394C>G , CM000667.1:g.125928394C>G	GRCh37
NC_000005.8:g.125956293C>G	NCBI36
NG_008600.2:g.7689G>C
NG_008600.3:g.7689G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409134.8:c.274G>C MANE Select	ENSP00000387123.3:p.Val92Leu
ENST00000412186.2:c.274G>C	ENSP00000414536.2:p.Val92Leu
ENST00000413020.6:c.274G>C	ENSP00000487936.1:p.Val92Leu
ENST00000458249.6:c.*183G>C	ENSP00000403929.1:n.*183G>C
ENST00000479989.6:n.457G>C
ENST00000503281.6:c.106+2305G>C
ENST00000509270.2:c.246+649G>C	ENSP00000449318.2:n.246+649G>C
ENST00000509459.6:c.65+2305G>C
ENST00000511266.6:n.996G>C
ENST00000635851.1:c.272G>C
ENST00000635858.1:n.113G>C
ENST00000635933.1:n.303G>C
ENST00000636062.1:n.169G>C
ENST00000636190.1:n.153G>C
ENST00000636225.1:c.*83G>C	ENSP00000490797.1:n.*83G>C
ENST00000636743.1:c.192+2305G>C	ENSP00000489725.1:n.192+2305G>C
ENST00000636808.1:c.*83G>C	ENSP00000490833.1:n.*83G>C
ENST00000636872.1:c.434G>C	ENSP00000490919.1:n.434G>C
ENST00000636879.1:c.274G>C	ENSP00000490811.1:p.Val92Leu
ENST00000636886.1:c.192+2305G>C	ENSP00000490371.1:n.192+2305G>C
ENST00000637206.1:c.274G>C	ENSP00000489895.1:p.Val92Leu
ENST00000637272.1:c.274G>C	ENSP00000489686.1:p.Val92Leu
ENST00000637782.1:c.274G>C	ENSP00000490024.1:p.Val92Leu
ENST00000637964.1:c.220G>C	ENSP00000490291.1:p.Val74Leu
ENST00000638008.1:c.*83G>C	ENSP00000490400.1:n.*83G>C
ENST00000409134.7:c.274G>C	ENSP00000387123.3:p.Val92Leu
ENST00000412186.1:c.*83G>C	ENSP00000414536.1:n.*83G>C
ENST00000413020.5:c.274G>C	ENSP00000487936.1:p.Val92Leu
ENST00000447989.6:c.355G>C	ENSP00000414132.2:p.Val119Leu
ENST00000458249.5:c.434G>C	ENSP00000403929.1:n.434G>C
ENST00000479989.5:n.457G>C
ENST00000503281.5:c.106+2305G>C
ENST00000509270.1:c.192+2305G>C	ENSP00000449318.1:n.192+2305G>C
ENST00000509459.5:c.65+2305G>C
ENST00000510111.6:c.268G>C	ENSP00000447388.1:p.Val90Leu
ENST00000511266.5:n.229G>C
ENST00000553117.5:c.274G>C	ENSP00000448593.1:p.Val92Leu
NM_001182.4:c.274G>C	NP_001173.2:p.Val92Leu
NM_001201377.1:c.190G>C	NP_001188306.1:p.Val64Leu
NM_001202404.1:c.355G>C	NP_001189333.1:p.Val119Leu
XM_011543417.1:c.-132G>C	XP_011541719.1:n.-132G>C
XM_011543417.2:c.-132G>C	XP_011541719.1:n.-132G>C
NM_001182.5:c.274G>C MANE Select	NP_001173.2:p.Val92Leu
NM_001201377.2:c.190G>C	NP_001188306.1:p.Val64Leu
NM_001202404.2:c.274G>C	NP_001189333.2:p.Val92Leu