Canonical Allele Identifier: CA488457387

Gene: ADSS1

Linked Data

• MyVariant Identifiers: chr14:g.105207576C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.104741239C>T , CM000676.2:g.104741239C>T	GRCh38
NC_000014.8:g.105207576C>T , CM000676.1:g.105207576C>T	GRCh37
NC_000014.7:g.104278621C>T	NCBI36
NG_051175.1:g.22043C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000710323.1:c.789C>T	ENSP00000518203.1:p.Asp263=
ENST00000330877.7:c.789C>T MANE Select	ENSP00000331260.2:p.Asp263=
ENST00000330877.6:c.789C>T	ENSP00000331260.2:p.Asp263=
ENST00000332972.9:c.918C>T	ENSP00000333019.5:p.Asp306=
ENST00000553540.5:c.901C>T	ENSP00000450759.1:n.901C>T
ENST00000555486.5:c.854C>T	ENSP00000473778.1:n.854C>T
ENST00000557582.5:n.1710C>T
NM_152328.3:c.789C>T	NP_689541.1:p.Asp263=
NM_199165.1:c.918C>T	NP_954634.1:p.Asp306=
XM_006720026.2:c.792C>T	XP_006720089.1:p.Asp264=
XM_011536412.1:c.921C>T	XP_011534714.1:p.Asp307=
XM_011536413.1:c.606C>T	XP_011534715.1:p.Asp202=
XM_011536414.1:c.603C>T	XP_011534716.1:p.Asp201=
XM_011536415.1:c.174C>T	XP_011534717.1:p.Asp58=
NM_001320424.1:c.174C>T	NP_001307353.1:p.Asp58=
NM_152328.4:c.789C>T	NP_689541.1:p.Asp263=
NM_199165.2:c.918C>T	NP_954634.1:p.Asp306=
XM_006720026.3:c.792C>T	XP_006720089.1:p.Asp264=
XM_011536412.2:c.921C>T	XP_011534714.1:p.Asp307=
XR_001750917.1:n.470G>A
NM_152328.5:c.789C>T MANE Select	NP_689541.1:p.Asp263=