Canonical Allele Identifier: CA375229468

Gene: ASS1

Linked Data

• MyVariant Identifiers: chr9:g.133355801T>A (hg19) ; chr9:g.130480414T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130480414T>A , CM000671.2:g.130480414T>A	GRCh38
NC_000009.11:g.133355801T>A , CM000671.1:g.133355801T>A	GRCh37
NC_000009.10:g.132345622T>A	NCBI36
NG_011542.1:g.40708T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.803T>A MANE Select	ENSP00000253004.6:p.Ile268Asn
ENST00000352480.9:c.803T>A	ENSP00000253004.6:p.Ile268Asn
ENST00000372386.6:n.74T>A
ENST00000372393.7:c.803T>A	ENSP00000361469.2:p.Ile268Asn
ENST00000372394.5:c.803T>A	ENSP00000361471.1:p.Ile268Asn
ENST00000470849.4:n.528T>A
ENST00000492400.5:n.312T>A
ENST00000493984.6:n.580T>A
NM_000050.4:c.803T>A	NP_000041.2:p.Ile268Asn
NM_054012.3:c.803T>A	NP_446464.1:p.Ile268Asn
XM_005272200.2:c.803T>A	XP_005272257.1:p.Ile268Asn
XM_011518705.1:c.917T>A	XP_011517007.1:p.Ile306Asn
XM_005272200.3:c.803T>A	XP_005272257.1:p.Ile268Asn
XM_011518705.2:c.917T>A	XP_011517007.1:p.Ile306Asn
XM_017014729.1:c.899T>A	XP_016870218.1:p.Ile300Asn
NM_054012.4:c.803T>A MANE Select	NP_446464.1:p.Ile268Asn