Canonical Allele Identifier: CA375229467

Gene: ASS1

Linked Data

• MyVariant Identifiers: chr9:g.133355800A>T (hg19) ; chr9:g.130480413A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130480413A>T , CM000671.2:g.130480413A>T	GRCh38
NC_000009.11:g.133355800A>T , CM000671.1:g.133355800A>T	GRCh37
NC_000009.10:g.132345621A>T	NCBI36
NG_011542.1:g.40707A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.802A>T MANE Select	ENSP00000253004.6:p.Ile268Phe
ENST00000352480.9:c.802A>T	ENSP00000253004.6:p.Ile268Phe
ENST00000372386.6:n.73A>T
ENST00000372393.7:c.802A>T	ENSP00000361469.2:p.Ile268Phe
ENST00000372394.5:c.802A>T	ENSP00000361471.1:p.Ile268Phe
ENST00000470849.4:n.527A>T
ENST00000492400.5:n.311A>T
ENST00000493984.6:n.579A>T
NM_000050.4:c.802A>T	NP_000041.2:p.Ile268Phe
NM_054012.3:c.802A>T	NP_446464.1:p.Ile268Phe
XM_005272200.2:c.802A>T	XP_005272257.1:p.Ile268Phe
XM_011518705.1:c.916A>T	XP_011517007.1:p.Ile306Phe
XM_005272200.3:c.802A>T	XP_005272257.1:p.Ile268Phe
XM_011518705.2:c.916A>T	XP_011517007.1:p.Ile306Phe
XM_017014729.1:c.898A>T	XP_016870218.1:p.Ile300Phe
NM_054012.4:c.802A>T MANE Select	NP_446464.1:p.Ile268Phe