Canonical Allele Identifier: CA200586080

Gene: ASS1

Linked Data

• dbSNP Id: rs756773327
• gnomAD v3: 9-130486565-G-C
• gnomAD v4: 9-130486565-G-C
• MyVariant Identifiers: chr9:g.133361952G>C (hg19) ; chr9:g.130486565G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130486565G>C , CM000671.2:g.130486565G>C	GRCh38
NC_000009.11:g.133361952G>C , CM000671.1:g.133361952G>C	GRCh37
NC_000009.10:g.132351773G>C	NCBI36
NG_011542.1:g.46859G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.839-2768G>C MANE Select	ENSP00000253004.6:n.839-2768G>C
ENST00000352480.9:c.839-2768G>C	ENSP00000253004.6:n.839-2768G>C
ENST00000372386.6:n.110-2768G>C
ENST00000372393.7:c.839-2768G>C	ENSP00000361469.2:n.839-2768G>C
ENST00000372394.5:c.839-2768G>C	ENSP00000361471.1:n.839-2768G>C
ENST00000470849.4:n.564-2768G>C
ENST00000492400.5:n.348-2768G>C
ENST00000493984.6:n.616-2768G>C
NM_000050.4:c.839-2768G>C	NP_000041.2:n.839-2768G>C
NM_054012.3:c.839-2768G>C	NP_446464.1:n.839-2768G>C
XM_005272200.2:c.839-2768G>C	XP_005272257.1:n.839-2768G>C
XM_011518705.1:c.953-2768G>C	XP_011517007.1:n.953-2768G>C
XM_005272200.3:c.839-2768G>C	XP_005272257.1:n.839-2768G>C
XM_011518705.2:c.953-2768G>C	XP_011517007.1:n.953-2768G>C
XM_017014729.1:c.935-2768G>C	XP_016870218.1:n.935-2768G>C
NM_054012.4:c.839-2768G>C MANE Select	NP_446464.1:n.839-2768G>C