Canonical Allele Identifier: CA1881271897

Gene: ASS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130480398G= , CM000671.2:g.130480398G=	GRCh38
NC_000009.11:g.133355785G= , CM000671.1:g.133355785G=	GRCh37
NC_000009.10:g.132345606G=	NCBI36
NG_011542.1:g.40692G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.787G= MANE Select	ENSP00000253004.6:p.Val263=
ENST00000352480.9:c.787G=	ENSP00000253004.6:p.Val263=
ENST00000372386.6:n.58G=
ENST00000372393.7:c.787G=	ENSP00000361469.2:p.Val263=
ENST00000372394.5:c.787G=	ENSP00000361471.1:p.Val263=
ENST00000470849.4:n.512G=
ENST00000492400.5:n.296G=
ENST00000493984.6:n.564G=
NM_000050.4:c.787G=	NP_000041.2:p.Val263=
NM_054012.3:c.787G=	NP_446464.1:p.Val263=
XM_005272200.2:c.787G=	XP_005272257.1:p.Val263=
XM_011518705.1:c.901G=	XP_011517007.1:p.Val301=
XM_005272200.3:c.787G=	XP_005272257.1:p.Val263=
XM_011518705.2:c.901G=	XP_011517007.1:p.Val301=
XM_017014729.1:c.883G=	XP_016870218.1:p.Val295=
NM_054012.4:c.787G= MANE Select	NP_446464.1:p.Val263=