Canonical Allele Identifier: CA1881276649

Gene: ASS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130489411T= , CM000671.2:g.130489411T=	GRCh38
NC_000009.11:g.133364798T= , CM000671.1:g.133364798T=	GRCh37
NC_000009.10:g.132354619T=	NCBI36
NG_011542.1:g.49705T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.917T= MANE Select	ENSP00000253004.6:p.Val306=
ENST00000352480.9:c.917T=	ENSP00000253004.6:p.Val306=
ENST00000372386.6:n.188T=
ENST00000372393.7:c.917T=	ENSP00000361469.2:p.Val306=
ENST00000372394.5:c.917T=	ENSP00000361471.1:p.Val306=
ENST00000470849.4:n.642T=
ENST00000492400.5:n.426T=
NM_000050.4:c.917T=	NP_000041.2:p.Val306=
NM_054012.3:c.917T=	NP_446464.1:p.Val306=
XM_005272200.2:c.917T=	XP_005272257.1:p.Val306=
XM_011518705.1:c.1031T=	XP_011517007.1:p.Val344=
XM_005272200.3:c.917T=	XP_005272257.1:p.Val306=
XM_011518705.2:c.1031T=	XP_011517007.1:p.Val344=
XM_017014729.1:c.1013T=	XP_016870218.1:p.Val338=
NM_054012.4:c.917T= MANE Select	NP_446464.1:p.Val306=