Canonical Allele Identifier: CA1881271714

Gene: ASS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130480199T= , CM000671.2:g.130480199T=	GRCh38
NC_000009.11:g.133355586T= , CM000671.1:g.133355586T=	GRCh37
NC_000009.10:g.132345407T=	NCBI36
NG_011542.1:g.40493T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.774-186T= MANE Select	ENSP00000253004.6:n.774-186T=
ENST00000352480.9:c.774-186T=	ENSP00000253004.6:n.774-186T=
ENST00000372386.6:n.45-186T=
ENST00000372393.7:c.774-186T=	ENSP00000361469.2:n.774-186T=
ENST00000372394.5:c.774-186T=	ENSP00000361471.1:n.774-186T=
ENST00000470849.4:n.499-186T=
ENST00000492400.5:n.283-186T=
ENST00000493984.6:n.551-186T=
NM_000050.4:c.774-186T=	NP_000041.2:n.774-186T=
NM_054012.3:c.774-186T=	NP_446464.1:n.774-186T=
XM_005272200.2:c.774-186T=	XP_005272257.1:n.774-186T=
XM_011518705.1:c.888-186T=	XP_011517007.1:n.888-186T=
XM_005272200.3:c.774-186T=	XP_005272257.1:n.774-186T=
XM_011518705.2:c.888-186T=	XP_011517007.1:n.888-186T=
XM_017014729.1:c.870-186T=	XP_016870218.1:n.870-186T=
NM_054012.4:c.774-186T= MANE Select	NP_446464.1:n.774-186T=