Canonical Allele Identifier: CA2160932381

Gene: ADSS1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.104741217A= , CM000676.2:g.104741217A=	GRCh38
NC_000014.8:g.105207554A= , CM000676.1:g.105207554A=	GRCh37
NC_000014.7:g.104278599A=	NCBI36
NG_051175.1:g.22021A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710323.1:c.767A=	ENSP00000518203.1:p.Asn256=
ENST00000330877.7:c.767A= MANE Select	ENSP00000331260.2:p.Asn256=
ENST00000330877.6:c.767A=	ENSP00000331260.2:p.Asn256=
ENST00000332972.9:c.896A=	ENSP00000333019.5:p.Asn299=
ENST00000553540.5:c.879A=	ENSP00000450759.1:n.879A=
ENST00000555486.5:c.832A=	ENSP00000473778.1:n.832A=
ENST00000557582.5:n.1688A=
NM_152328.3:c.767A=	NP_689541.1:p.Asn256=
NM_199165.1:c.896A=	NP_954634.1:p.Asn299=
XM_006720026.2:c.770A=	XP_006720089.1:p.Asn257=
XM_011536412.1:c.899A=	XP_011534714.1:p.Asn300=
XM_011536413.1:c.584A=	XP_011534715.1:p.Asn195=
XM_011536414.1:c.581A=	XP_011534716.1:p.Asn194=
XM_011536415.1:c.152A=	XP_011534717.1:p.Asn51=
NM_001320424.1:c.152A=	NP_001307353.1:p.Asn51=
NM_152328.4:c.767A=	NP_689541.1:p.Asn256=
NM_199165.2:c.896A=	NP_954634.1:p.Asn299=
XM_006720026.3:c.770A=	XP_006720089.1:p.Asn257=
XM_011536412.2:c.899A=	XP_011534714.1:p.Asn300=
XR_001750917.1:n.492T=
NM_152328.5:c.767A= MANE Select	NP_689541.1:p.Asn256=