Canonical Allele Identifier: CA1881248174

Gene: ASS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130455992G= , CM000671.2:g.130455992G=	GRCh38
NC_000009.11:g.133331379G= , CM000671.1:g.133331379G=	GRCh37
NC_000009.10:g.132321200G=	NCBI36
NG_011542.1:g.16286G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.174+1619G= MANE Select	ENSP00000253004.6:n.174+1619G=
ENST00000352480.9:c.174+1619G=	ENSP00000253004.6:n.174+1619G=
ENST00000372393.7:c.174+1619G=	ENSP00000361469.2:n.174+1619G=
ENST00000372394.5:c.174+1619G=	ENSP00000361471.1:n.174+1619G=
ENST00000422569.5:c.174+1619G=	ENSP00000394212.1:n.174+1619G=
ENST00000443588.1:c.174+1619G=	ENSP00000397785.1:n.174+1619G=
NM_000050.4:c.174+1619G=	NP_000041.2:n.174+1619G=
NM_054012.3:c.174+1619G=	NP_446464.1:n.174+1619G=
XM_005272200.2:c.174+1619G=	XP_005272257.1:n.174+1619G=
XM_011518705.1:c.288+1619G=	XP_011517007.1:n.288+1619G=
XM_005272200.3:c.174+1619G=	XP_005272257.1:n.174+1619G=
XM_011518705.2:c.288+1619G=	XP_011517007.1:n.288+1619G=
XM_017014729.1:c.270+1619G=	XP_016870218.1:n.270+1619G=
NM_054012.4:c.174+1619G= MANE Select	NP_446464.1:n.174+1619G=