Canonical Allele Identifier: CA2556464651

Gene: ARSL

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.2934841del , CM000685.2:g.2934841del	GRCh38
NC_000023.10:g.2852882del , CM000685.1:g.2852882del	GRCh37
NC_000023.9:g.2862882del	NCBI36
NG_007091.1:g.34432del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540563.6:c.1763del	ENSP00000438198.2:p.Pro588HisfsTer7
ENST00000681963.1:c.1838del	ENSP00000507760.1:p.Pro613HisfsTer7
ENST00000682184.1:c.1640del	ENSP00000507043.1:p.Pro547HisfsTer7
ENST00000682364.1:c.1202del	ENSP00000507604.1:p.Pro401HisfsTer?
ENST00000683191.1:n.1543del
ENST00000683290.1:c.1838del	ENSP00000508156.1:p.Pro613HisfsTer7
ENST00000683677.1:c.1751del	ENSP00000506786.1:p.Pro584HisfsTer7
ENST00000684077.1:c.1316del	ENSP00000506767.1:p.Pro439HisfsTer?
ENST00000684117.1:c.1601del	ENSP00000508337.1:p.Pro534HisfsTer7
ENST00000684364.1:c.1751del	ENSP00000507304.1:p.Pro584HisfsTer7
ENST00000684738.1:c.1202del	ENSP00000507481.1:p.Pro401HisfsTer?
ENST00000381134.9:c.1763del MANE Select	ENSP00000370526.3:p.Pro588HisfsTer7
ENST00000545496.6:c.1838del	ENSP00000441417.1:p.Pro613HisfsTer7
ENST00000672027.1:c.1838del	ENSP00000500220.1:p.Pro613HisfsTer?
ENST00000672097.1:c.1760del	ENSP00000500727.1:p.Pro587HisfsTer7
ENST00000672761.1:c.1601del	ENSP00000500108.1:p.Pro534HisfsTer7
ENST00000673032.1:c.1601del	ENSP00000500778.1:p.Pro534HisfsTer7
ENST00000381134.7:c.1763del	ENSP00000370526.3:p.Pro588HisfsTer7
ENST00000540563.5:c.1628del	ENSP00000438198.1:p.Pro543HisfsTer7
ENST00000545496.5:c.1838del	ENSP00000441417.1:p.Pro613HisfsTer7
NM_000047.2:c.1763del	NP_000038.2:p.Pro588HisfsTer7
NM_001282628.1:c.1838del	NP_001269557.1:p.Pro613HisfsTer7
NM_001282631.1:c.1628del	NP_001269560.1:p.Pro543HisfsTer7
XM_005274518.2:c.1790del	XP_005274575.1:p.Pro597HisfsTer7
XM_005274519.3:c.1763del	XP_005274576.1:p.Pro588HisfsTer7
XM_005274521.3:c.1601del	XP_005274578.1:p.Pro534HisfsTer7
XM_011545519.1:c.1601del	XP_011543821.1:p.Pro534HisfsTer7
XM_011545520.1:c.1277del	XP_011543822.1:p.Pro426HisfsTer7
XM_011545521.1:c.1202del	XP_011543823.1:p.Pro401HisfsTer7
XM_005274519.4:c.1763del	XP_005274576.1:p.Pro588HisfsTer7
XM_005274521.4:c.1601del	XP_005274578.1:p.Pro534HisfsTer7
XM_017029525.1:c.1838del	XP_016885014.1:p.Pro613HisfsTer7
XM_017029526.1:c.1277del	XP_016885015.1:p.Pro426HisfsTer7
NM_000047.3:c.1763del MANE Select	NP_000038.2:p.Pro588HisfsTer7
NM_001282631.2:c.1601del	NP_001269560.2:p.Pro534HisfsTer7
NM_001369079.1:c.1790del	NP_001356008.1:p.Pro597HisfsTer7
NM_001369080.1:c.1838del	NP_001356009.1:p.Pro613HisfsTer7
NM_001282628.2:c.1838del	NP_001269557.1:p.Pro613HisfsTer7