Canonical Allele Identifier: CA375229454

Gene: ASS1

Linked Data

• dbSNP Id: rs1846140663
• MyVariant Identifiers: chr9:g.133355795T>C (hg19) ; chr9:g.130480408T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130480408T>C , CM000671.2:g.130480408T>C	GRCh38
NC_000009.11:g.133355795T>C , CM000671.1:g.133355795T>C	GRCh37
NC_000009.10:g.132345616T>C	NCBI36
NG_011542.1:g.40702T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.797T>C MANE Select	ENSP00000253004.6:p.Ile266Thr
ENST00000352480.9:c.797T>C	ENSP00000253004.6:p.Ile266Thr
ENST00000372386.6:n.68T>C
ENST00000372393.7:c.797T>C	ENSP00000361469.2:p.Ile266Thr
ENST00000372394.5:c.797T>C	ENSP00000361471.1:p.Ile266Thr
ENST00000470849.4:n.522T>C
ENST00000492400.5:n.306T>C
ENST00000493984.6:n.574T>C
NM_000050.4:c.797T>C	NP_000041.2:p.Ile266Thr
NM_054012.3:c.797T>C	NP_446464.1:p.Ile266Thr
XM_005272200.2:c.797T>C	XP_005272257.1:p.Ile266Thr
XM_011518705.1:c.911T>C	XP_011517007.1:p.Ile304Thr
XM_005272200.3:c.797T>C	XP_005272257.1:p.Ile266Thr
XM_011518705.2:c.911T>C	XP_011517007.1:p.Ile304Thr
XM_017014729.1:c.893T>C	XP_016870218.1:p.Ile298Thr
NM_054012.4:c.797T>C MANE Select	NP_446464.1:p.Ile266Thr