Canonical Allele Identifier: CA2160932241

Gene: ADSS1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.104741016C= , CM000676.2:g.104741016C=	GRCh38
NC_000014.8:g.105207353C= , CM000676.1:g.105207353C=	GRCh37
NC_000014.7:g.104278398C=	NCBI36
NG_051175.1:g.21820C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710323.1:c.666+96C=	ENSP00000518203.1:n.666+96C=
ENST00000330877.7:c.666+96C= MANE Select	ENSP00000331260.2:n.666+96C=
ENST00000330877.6:c.666+96C=	ENSP00000331260.2:n.666+96C=
ENST00000332972.9:c.795+96C=	ENSP00000333019.5:n.795+96C=
ENST00000553540.5:c.778+96C=	ENSP00000450759.1:n.778+96C=
ENST00000555486.5:c.731+96C=	ENSP00000473778.1:n.731+96C=
ENST00000557582.5:n.1587+96C=
NM_152328.3:c.666+96C=	NP_689541.1:n.666+96C=
NM_199165.1:c.795+96C=	NP_954634.1:n.795+96C=
XM_006720026.2:c.669+96C=	XP_006720089.1:n.669+96C=
XM_011536412.1:c.798+96C=	XP_011534714.1:n.798+96C=
XM_011536413.1:c.483+96C=	XP_011534715.1:n.483+96C=
XM_011536414.1:c.480+96C=	XP_011534716.1:n.480+96C=
XM_011536415.1:c.51+96C=	XP_011534717.1:n.51+96C=
NM_001320424.1:c.51+96C=	NP_001307353.1:n.51+96C=
NM_152328.4:c.666+96C=	NP_689541.1:n.666+96C=
NM_199165.2:c.795+96C=	NP_954634.1:n.795+96C=
XM_006720026.3:c.669+96C=	XP_006720089.1:n.669+96C=
XM_011536412.2:c.798+96C=	XP_011534714.1:n.798+96C=
NM_152328.5:c.666+96C= MANE Select	NP_689541.1:n.666+96C=