Canonical Allele Identifier: CA1881276662

Gene: ASS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130489437T= , CM000671.2:g.130489437T=	GRCh38
NC_000009.11:g.133364824T= , CM000671.1:g.133364824T=	GRCh37
NC_000009.10:g.132354645T=	NCBI36
NG_011542.1:g.49731T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.943T= MANE Select	ENSP00000253004.6:p.Leu315=
ENST00000352480.9:c.943T=	ENSP00000253004.6:p.Leu315=
ENST00000372386.6:n.214T=
ENST00000372393.7:c.943T=	ENSP00000361469.2:p.Leu315=
ENST00000372394.5:c.943T=	ENSP00000361471.1:p.Leu315=
NM_000050.4:c.943T=	NP_000041.2:p.Leu315=
NM_054012.3:c.943T=	NP_446464.1:p.Leu315=
XM_005272200.2:c.943T=	XP_005272257.1:p.Leu315=
XM_011518705.1:c.1057T=	XP_011517007.1:p.Leu353=
XM_005272200.3:c.943T=	XP_005272257.1:p.Leu315=
XM_011518705.2:c.1057T=	XP_011517007.1:p.Leu353=
XM_017014729.1:c.1039T=	XP_016870218.1:p.Leu347=
NM_054012.4:c.943T= MANE Select	NP_446464.1:p.Leu315=