Canonical Allele Identifier: CA1881271980

Gene: ASS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130480433T= , CM000671.2:g.130480433T=	GRCh38
NC_000009.11:g.133355820T= , CM000671.1:g.133355820T=	GRCh37
NC_000009.10:g.132345641T=	NCBI36
NG_011542.1:g.40727T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.822T= MANE Select	ENSP00000253004.6:p.Ile274=
ENST00000352480.9:c.822T=	ENSP00000253004.6:p.Ile274=
ENST00000372386.6:n.93T=
ENST00000372393.7:c.822T=	ENSP00000361469.2:p.Ile274=
ENST00000372394.5:c.822T=	ENSP00000361471.1:p.Ile274=
ENST00000470849.4:n.547T=
ENST00000492400.5:n.331T=
ENST00000493984.6:n.599T=
NM_000050.4:c.822T=	NP_000041.2:p.Ile274=
NM_054012.3:c.822T=	NP_446464.1:p.Ile274=
XM_005272200.2:c.822T=	XP_005272257.1:p.Ile274=
XM_011518705.1:c.936T=	XP_011517007.1:p.Ile312=
XM_005272200.3:c.822T=	XP_005272257.1:p.Ile274=
XM_011518705.2:c.936T=	XP_011517007.1:p.Ile312=
XM_017014729.1:c.918T=	XP_016870218.1:p.Ile306=
NM_054012.4:c.822T= MANE Select	NP_446464.1:p.Ile274=