Canonical Allele Identifier: CA5283541

Gene: ASS1

Linked Data

• ClinVar Variation Id: 1530674
• ClinVar RCV Id: RCV002089840
• dbSNP Id: rs760468184
• ExAC: 9:133355845 G / A
• gnomAD v2: 9-133355845-G-A
• gnomAD v3: 9-130480458-G-A
• gnomAD v4: 9-130480458-G-A
• MyVariant Identifiers: chr9:g.133355845G>A (hg19) ; chr9:g.130480458G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130480458G>A , CM000671.2:g.130480458G>A	GRCh38
NC_000009.11:g.133355845G>A , CM000671.1:g.133355845G>A	GRCh37
NC_000009.10:g.132345666G>A	NCBI36
NG_011542.1:g.40752G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.838+9G>A MANE Select	ENSP00000253004.6:n.838+9G>A
ENST00000352480.9:c.838+9G>A	ENSP00000253004.6:n.838+9G>A
ENST00000372386.6:n.109+9G>A
ENST00000372393.7:c.838+9G>A	ENSP00000361469.2:n.838+9G>A
ENST00000372394.5:c.838+9G>A	ENSP00000361471.1:n.838+9G>A
ENST00000470849.4:n.563+9G>A
ENST00000492400.5:n.347+9G>A
ENST00000493984.6:n.615+9G>A
NM_000050.4:c.838+9G>A	NP_000041.2:n.838+9G>A
NM_054012.3:c.838+9G>A	NP_446464.1:n.838+9G>A
XM_005272200.2:c.838+9G>A	XP_005272257.1:n.838+9G>A
XM_011518705.1:c.952+9G>A	XP_011517007.1:n.952+9G>A
XM_005272200.3:c.838+9G>A	XP_005272257.1:n.838+9G>A
XM_011518705.2:c.952+9G>A	XP_011517007.1:n.952+9G>A
XM_017014729.1:c.934+9G>A	XP_016870218.1:n.934+9G>A
NM_054012.4:c.838+9G>A MANE Select	NP_446464.1:n.838+9G>A