Canonical Allele Identifier: CA1881281176

Gene: ASS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130499515C= , CM000671.2:g.130499515C=	GRCh38
NC_000009.11:g.133374902C= , CM000671.1:g.133374902C=	GRCh37
NC_000009.10:g.132364723C=	NCBI36
NG_011542.1:g.59809C=

Transcript Alleles

HGVS	Amino-acid Change
NM_054012.4:c.1138C= MANE Select	NP_446464.1:p.Gln380=
ENST00000352480.10:c.1138C= MANE Select	ENSP00000253004.6:p.Gln380=
NM_000050.4:c.1138C=	NP_000041.2:p.Gln380=
NM_054012.3:c.1138C=	NP_446464.1:p.Gln380=
ENST00000352480.9:c.1138C=	ENSP00000253004.6:p.Gln380=
ENST00000372386.6:n.409C=
ENST00000372393.7:c.1138C=	ENSP00000361469.2:p.Gln380=
ENST00000372394.5:c.1138C=	ENSP00000361471.1:p.Gln380=
XM_005272200.2:c.1138C=	XP_005272257.1:p.Gln380=
XM_005272200.3:c.1138C=	XP_005272257.1:p.Gln380=
XM_011518705.1:c.1252C=	XP_011517007.1:p.Gln418=
XM_011518705.2:c.1252C=	XP_011517007.1:p.Gln418=
XM_017014729.1:c.1234C=	XP_016870218.1:p.Gln412=
XR_930393.1:n.1059+432G=
XR_930393.2:n.1101+432G=