Canonical Allele Identifier: CA2160932291

Gene: ADSS1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.104741129C= , CM000676.2:g.104741129C=	GRCh38
NC_000014.8:g.105207466C= , CM000676.1:g.105207466C=	GRCh37
NC_000014.7:g.104278511C=	NCBI36
NG_051175.1:g.21933C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710323.1:c.679C=	ENSP00000518203.1:p.Arg227=
ENST00000330877.7:c.679C= MANE Select	ENSP00000331260.2:p.Arg227=
ENST00000330877.6:c.679C=	ENSP00000331260.2:p.Arg227=
ENST00000332972.9:c.808C=	ENSP00000333019.5:p.Arg270=
ENST00000553540.5:c.791C=	ENSP00000450759.1:n.791C=
ENST00000555486.5:c.744C=	ENSP00000473778.1:n.744C=
ENST00000557582.5:n.1600C=
NM_152328.3:c.679C=	NP_689541.1:p.Arg227=
NM_199165.1:c.808C=	NP_954634.1:p.Arg270=
XM_006720026.2:c.682C=	XP_006720089.1:p.Arg228=
XM_011536412.1:c.811C=	XP_011534714.1:p.Arg271=
XM_011536413.1:c.496C=	XP_011534715.1:p.Arg166=
XM_011536414.1:c.493C=	XP_011534716.1:p.Arg165=
XM_011536415.1:c.64C=	XP_011534717.1:p.Arg22=
NM_001320424.1:c.64C=	NP_001307353.1:p.Arg22=
NM_152328.4:c.679C=	NP_689541.1:p.Arg227=
NM_199165.2:c.808C=	NP_954634.1:p.Arg270=
XM_006720026.3:c.682C=	XP_006720089.1:p.Arg228=
XM_011536412.2:c.811C=	XP_011534714.1:p.Arg271=
NM_152328.5:c.679C= MANE Select	NP_689541.1:p.Arg227=