Canonical Allele Identifier: CA2579543783

Gene: ARSL

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.2934851del , CM000685.2:g.2934851del	GRCh38
NC_000023.10:g.2852892del , CM000685.1:g.2852892del	GRCh37
NC_000023.9:g.2862892del	NCBI36
NG_007091.1:g.34422del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540563.6:c.1753del	ENSP00000438198.2:p.Glu585LysfsTer10
ENST00000681963.1:c.1828del	ENSP00000507760.1:p.Glu610LysfsTer10
ENST00000682184.1:c.1630del	ENSP00000507043.1:p.Glu544LysfsTer10
ENST00000682364.1:c.1192del	ENSP00000507604.1:p.Glu398LysfsTer?
ENST00000683191.1:n.1533del
ENST00000683290.1:c.1828del	ENSP00000508156.1:p.Glu610LysfsTer10
ENST00000683677.1:c.1741del	ENSP00000506786.1:p.Glu581LysfsTer10
ENST00000684077.1:c.1306del	ENSP00000506767.1:p.Glu436LysfsTer?
ENST00000684117.1:c.1591del	ENSP00000508337.1:p.Glu531LysfsTer10
ENST00000684364.1:c.1741del	ENSP00000507304.1:p.Glu581LysfsTer10
ENST00000684738.1:c.1192del	ENSP00000507481.1:p.Glu398LysfsTer?
ENST00000381134.9:c.1753del MANE Select	ENSP00000370526.3:p.Glu585LysfsTer10
ENST00000545496.6:c.1828del	ENSP00000441417.1:p.Glu610LysfsTer10
ENST00000672027.1:c.1828del	ENSP00000500220.1:p.Glu610LysfsTer?
ENST00000672097.1:c.1750del	ENSP00000500727.1:p.Glu584LysfsTer10
ENST00000672761.1:c.1591del	ENSP00000500108.1:p.Glu531LysfsTer10
ENST00000673032.1:c.1591del	ENSP00000500778.1:p.Glu531LysfsTer10
ENST00000381134.7:c.1753del	ENSP00000370526.3:p.Glu585LysfsTer10
ENST00000540563.5:c.1618del	ENSP00000438198.1:p.Glu540LysfsTer10
ENST00000545496.5:c.1828del	ENSP00000441417.1:p.Glu610LysfsTer10
NM_000047.2:c.1753del	NP_000038.2:p.Glu585LysfsTer10
NM_001282628.1:c.1828del	NP_001269557.1:p.Glu610LysfsTer10
NM_001282631.1:c.1618del	NP_001269560.1:p.Glu540LysfsTer10
XM_005274518.2:c.1780del	XP_005274575.1:p.Glu594LysfsTer10
XM_005274519.3:c.1753del	XP_005274576.1:p.Glu585LysfsTer10
XM_005274521.3:c.1591del	XP_005274578.1:p.Glu531LysfsTer10
XM_011545519.1:c.1591del	XP_011543821.1:p.Glu531LysfsTer10
XM_011545520.1:c.1267del	XP_011543822.1:p.Glu423LysfsTer10
XM_011545521.1:c.1192del	XP_011543823.1:p.Glu398LysfsTer10
XM_005274519.4:c.1753del	XP_005274576.1:p.Glu585LysfsTer10
XM_005274521.4:c.1591del	XP_005274578.1:p.Glu531LysfsTer10
XM_017029525.1:c.1828del	XP_016885014.1:p.Glu610LysfsTer10
XM_017029526.1:c.1267del	XP_016885015.1:p.Glu423LysfsTer10
NM_000047.3:c.1753del MANE Select	NP_000038.2:p.Glu585LysfsTer10
NM_001282631.2:c.1591del	NP_001269560.2:p.Glu531LysfsTer10
NM_001369079.1:c.1780del	NP_001356008.1:p.Glu594LysfsTer10
NM_001369080.1:c.1828del	NP_001356009.1:p.Glu610LysfsTer10
NM_001282628.2:c.1828del	NP_001269557.1:p.Glu610LysfsTer10