Canonical Allele Identifier: CA1881256300

Gene: ASS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130471514A= , CM000671.2:g.130471514A=	GRCh38
NC_000009.11:g.133346901A= , CM000671.1:g.133346901A=	GRCh37
NC_000009.10:g.132336722A=	NCBI36
NG_011542.1:g.31808A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352480.10:c.596A= MANE Select	ENSP00000253004.6:p.Lys199=
ENST00000352480.9:c.596A=	ENSP00000253004.6:p.Lys199=
ENST00000372393.7:c.596A=	ENSP00000361469.2:p.Lys199=
ENST00000372394.5:c.596A=	ENSP00000361471.1:p.Lys199=
ENST00000443588.1:c.539A=
ENST00000467695.5:n.305A=
ENST00000493984.6:n.427A=
NM_000050.4:c.596A=	NP_000041.2:p.Lys199=
NM_054012.3:c.596A=	NP_446464.1:p.Lys199=
XM_005272200.2:c.596A=	XP_005272257.1:p.Lys199=
XM_011518705.1:c.710A=	XP_011517007.1:p.Lys237=
XM_005272200.3:c.596A=	XP_005272257.1:p.Lys199=
XM_011518705.2:c.710A=	XP_011517007.1:p.Lys237=
XM_017014729.1:c.692A=	XP_016870218.1:p.Lys231=
NM_054012.4:c.596A= MANE Select	NP_446464.1:p.Lys199=