Canonical Allele Identifier: CA2412586999
Gene: ARSL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.2953247C= , CM000685.2:g.2953247C= GRCh38
NC_000023.10:g.2871288C= , CM000685.1:g.2871288C= GRCh37
NC_000023.9:g.2881288C= NCBI36
NG_007091.1:g.16024G=

Transcript Alleles

HGVS Amino-acid change
ENST00000483425.2:n.411G=
ENST00000540563.6:c.326G= ENSP00000438198.2:p.Gly109=
ENST00000681960.1:n.652G=
ENST00000681963.1:c.401G= ENSP00000507760.1:p.Gly134=
ENST00000682184.1:c.307+2169G= ENSP00000507043.1:n.307+2169G=
ENST00000682364.1:c.326G= ENSP00000507604.1:p.Gly109=
ENST00000682745.1:n.411G=
ENST00000683071.1:n.218G=
ENST00000683191.1:n.106G=
ENST00000683290.1:c.401G= ENSP00000508156.1:p.Gly134=
ENST00000683677.1:c.314G= ENSP00000506786.1:p.Gly105=
ENST00000683854.1:n.411G=
ENST00000683958.1:c.326G= ENSP00000507756.1:p.Gly109=
ENST00000684045.1:n.640G=
ENST00000684077.1:c.164G= ENSP00000506767.1:p.Gly55=
ENST00000684117.1:c.164G= ENSP00000508337.1:p.Gly55=
ENST00000684364.1:c.314G= ENSP00000507304.1:p.Gly105=
ENST00000684687.1:c.164G= ENSP00000507266.1:p.Gly55=
ENST00000684738.1:c.326G= ENSP00000507481.1:p.Gly109=
ENST00000381134.9:c.326G= MANE Select ENSP00000370526.3:p.Gly109=
ENST00000545496.6:c.401G= ENSP00000441417.1:p.Gly134=
ENST00000672027.1:c.401G= ENSP00000500220.1:p.Gly134=
ENST00000672097.1:c.326G= ENSP00000500727.1:p.Gly109=
ENST00000672606.1:c.326G= ENSP00000500638.1:p.Gly109=
ENST00000672761.1:c.164G= ENSP00000500108.1:p.Gly55=
ENST00000673032.1:c.164G= ENSP00000500778.1:p.Gly55=
ENST00000381134.7:c.326G= ENSP00000370526.3:p.Gly109=
ENST00000438544.5:c.326G= ENSP00000406528.1:p.Gly109=
ENST00000540563.5:c.191G= ENSP00000438198.1:p.Gly64=
ENST00000545496.5:c.401G= ENSP00000441417.1:p.Gly134=
NM_000047.2:c.326G= NP_000038.2:p.Gly109=
NM_001282628.1:c.401G= NP_001269557.1:p.Gly134=
NM_001282631.1:c.191G= NP_001269560.1:p.Gly64=
XM_005274518.2:c.353G= XP_005274575.1:p.Gly118=
XM_005274519.3:c.326G= XP_005274576.1:p.Gly109=
XM_005274521.3:c.164G= XP_005274578.1:p.Gly55=
XM_011545519.1:c.164G= XP_011543821.1:p.Gly55=
XM_011545520.1:c.401G= XP_011543822.1:p.Gly134=
XM_011545521.1:c.326G= XP_011543823.1:p.Gly109=
XM_005274519.4:c.326G= XP_005274576.1:p.Gly109=
XM_005274521.4:c.164G= XP_005274578.1:p.Gly55=
XM_017029525.1:c.401G= XP_016885014.1:p.Gly134=
XM_017029526.1:c.401G= XP_016885015.1:p.Gly134=
NM_000047.3:c.326G= MANE Select NP_000038.2:p.Gly109=
NM_001282631.2:c.164G= NP_001269560.2:p.Gly55=
NM_001369079.1:c.353G= NP_001356008.1:p.Gly118=
NM_001369080.1:c.401G= NP_001356009.1:p.Gly134=
NM_001282628.2:c.401G= NP_001269557.1:p.Gly134=