Canonical Allele Identifier: CA2412580487

Gene: ARSL

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.2934843C= , CM000685.2:g.2934843C=	GRCh38
NC_000023.10:g.2852884C= , CM000685.1:g.2852884C=	GRCh37
NC_000023.9:g.2862884C=	NCBI36
NG_007091.1:g.34428G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540563.6:c.1759G=	ENSP00000438198.2:p.Asp587=
ENST00000681963.1:c.1834G=	ENSP00000507760.1:p.Asp612=
ENST00000682184.1:c.1636G=	ENSP00000507043.1:p.Asp546=
ENST00000682364.1:c.1198G=	ENSP00000507604.1:p.Asp400=
ENST00000683191.1:n.1539G=
ENST00000683290.1:c.1834G=	ENSP00000508156.1:p.Asp612=
ENST00000683677.1:c.1747G=	ENSP00000506786.1:p.Asp583=
ENST00000684077.1:c.1312G=	ENSP00000506767.1:p.Asp438=
ENST00000684117.1:c.1597G=	ENSP00000508337.1:p.Asp533=
ENST00000684364.1:c.1747G=	ENSP00000507304.1:p.Asp583=
ENST00000684738.1:c.1198G=	ENSP00000507481.1:p.Asp400=
ENST00000381134.9:c.1759G= MANE Select	ENSP00000370526.3:p.Asp587=
ENST00000545496.6:c.1834G=	ENSP00000441417.1:p.Asp612=
ENST00000672027.1:c.1834G=	ENSP00000500220.1:p.Asp612=
ENST00000672097.1:c.1756G=	ENSP00000500727.1:p.Asp586=
ENST00000672761.1:c.1597G=	ENSP00000500108.1:p.Asp533=
ENST00000673032.1:c.1597G=	ENSP00000500778.1:p.Asp533=
ENST00000381134.7:c.1759G=	ENSP00000370526.3:p.Asp587=
ENST00000540563.5:c.1624G=	ENSP00000438198.1:p.Asp542=
ENST00000545496.5:c.1834G=	ENSP00000441417.1:p.Asp612=
NM_000047.2:c.1759G=	NP_000038.2:p.Asp587=
NM_001282628.1:c.1834G=	NP_001269557.1:p.Asp612=
NM_001282631.1:c.1624G=	NP_001269560.1:p.Asp542=
XM_005274518.2:c.1786G=	XP_005274575.1:p.Asp596=
XM_005274519.3:c.1759G=	XP_005274576.1:p.Asp587=
XM_005274521.3:c.1597G=	XP_005274578.1:p.Asp533=
XM_011545519.1:c.1597G=	XP_011543821.1:p.Asp533=
XM_011545520.1:c.1273G=	XP_011543822.1:p.Asp425=
XM_011545521.1:c.1198G=	XP_011543823.1:p.Asp400=
XM_005274519.4:c.1759G=	XP_005274576.1:p.Asp587=
XM_005274521.4:c.1597G=	XP_005274578.1:p.Asp533=
XM_017029525.1:c.1834G=	XP_016885014.1:p.Asp612=
XM_017029526.1:c.1273G=	XP_016885015.1:p.Asp425=
NM_000047.3:c.1759G= MANE Select	NP_000038.2:p.Asp587=
NM_001282631.2:c.1597G=	NP_001269560.2:p.Asp533=
NM_001369079.1:c.1786G=	NP_001356008.1:p.Asp596=
NM_001369080.1:c.1834G=	NP_001356009.1:p.Asp612=
NM_001282628.2:c.1834G=	NP_001269557.1:p.Asp612=