Canonical Allele Identifier: CA10632839

Gene: ASS1

Linked Data

• ClinVar Variation Id: 365261
• ClinVar RCV Id: RCV000339353
• dbSNP Id: rs886063532
• MyVariant Identifiers: chr9:g.133364863T>A (hg19) ; chr9:g.130489476T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130489476T>A , CM000671.2:g.130489476T>A	GRCh38
NC_000009.11:g.133364863T>A , CM000671.1:g.133364863T>A	GRCh37
NC_000009.10:g.132354684T>A	NCBI36
NG_011542.1:g.49770T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.970+12T>A MANE Select	ENSP00000253004.6:n.970+12T>A
ENST00000352480.9:c.970+12T>A	ENSP00000253004.6:n.970+12T>A
ENST00000372386.6:n.241+12T>A
ENST00000372393.7:c.970+12T>A	ENSP00000361469.2:n.970+12T>A
ENST00000372394.5:c.970+12T>A	ENSP00000361471.1:n.970+12T>A
NM_000050.4:c.970+12T>A	NP_000041.2:n.970+12T>A
NM_054012.3:c.970+12T>A	NP_446464.1:n.970+12T>A
XM_005272200.2:c.970+12T>A	XP_005272257.1:n.970+12T>A
XM_011518705.1:c.1084+12T>A	XP_011517007.1:n.1084+12T>A
XM_005272200.3:c.970+12T>A	XP_005272257.1:n.970+12T>A
XM_011518705.2:c.1084+12T>A	XP_011517007.1:n.1084+12T>A
XM_017014729.1:c.1066+12T>A	XP_016870218.1:n.1066+12T>A
NM_054012.4:c.970+12T>A MANE Select	NP_446464.1:n.970+12T>A