Canonical Allele Identifier: CA1881271976

Gene: ASS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130480426G= , CM000671.2:g.130480426G=	GRCh38
NC_000009.11:g.133355813G= , CM000671.1:g.133355813G=	GRCh37
NC_000009.10:g.132345634G=	NCBI36
NG_011542.1:g.40720G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.815G= MANE Select	ENSP00000253004.6:p.Arg272=
ENST00000352480.9:c.815G=	ENSP00000253004.6:p.Arg272=
ENST00000372386.6:n.86G=
ENST00000372393.7:c.815G=	ENSP00000361469.2:p.Arg272=
ENST00000372394.5:c.815G=	ENSP00000361471.1:p.Arg272=
ENST00000470849.4:n.540G=
ENST00000492400.5:n.324G=
ENST00000493984.6:n.592G=
NM_000050.4:c.815G=	NP_000041.2:p.Arg272=
NM_054012.3:c.815G=	NP_446464.1:p.Arg272=
XM_005272200.2:c.815G=	XP_005272257.1:p.Arg272=
XM_011518705.1:c.929G=	XP_011517007.1:p.Arg310=
XM_005272200.3:c.815G=	XP_005272257.1:p.Arg272=
XM_011518705.2:c.929G=	XP_011517007.1:p.Arg310=
XM_017014729.1:c.911G=	XP_016870218.1:p.Arg304=
NM_054012.4:c.815G= MANE Select	NP_446464.1:p.Arg272=