Canonical Allele Identifier: CA412267431

Gene: ARSL

Linked Data

• MyVariant Identifiers: chrX:g.2871193C>A (hg19) ; chrX:g.2953152C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.2953152C>A , CM000685.2:g.2953152C>A	GRCh38
NC_000023.10:g.2871193C>A , CM000685.1:g.2871193C>A	GRCh37
NC_000023.9:g.2881193C>A	NCBI36
NG_007091.1:g.16119G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483425.2:n.506G>T
ENST00000540563.6:c.421G>T	ENSP00000438198.2:p.Gly141Ter
ENST00000681960.1:n.747G>T
ENST00000681963.1:c.496G>T	ENSP00000507760.1:p.Gly166Ter
ENST00000682184.1:c.307+2264G>T	ENSP00000507043.1:n.307+2264G>T
ENST00000682364.1:c.421G>T	ENSP00000507604.1:p.Gly141Ter
ENST00000682745.1:n.506G>T
ENST00000683071.1:n.313G>T
ENST00000683191.1:n.201G>T
ENST00000683290.1:c.496G>T	ENSP00000508156.1:p.Gly166Ter
ENST00000683677.1:c.409G>T	ENSP00000506786.1:p.Gly137Ter
ENST00000683854.1:n.506G>T
ENST00000683958.1:c.421G>T	ENSP00000507756.1:p.Gly141Ter
ENST00000684045.1:n.735G>T
ENST00000684077.1:c.259G>T	ENSP00000506767.1:p.Gly87Ter
ENST00000684117.1:c.259G>T	ENSP00000508337.1:p.Gly87Ter
ENST00000684364.1:c.409G>T	ENSP00000507304.1:p.Gly137Ter
ENST00000684687.1:c.259G>T	ENSP00000507266.1:p.Gly87Ter
ENST00000684738.1:c.421G>T	ENSP00000507481.1:p.Gly141Ter
ENST00000381134.9:c.421G>T MANE Select	ENSP00000370526.3:p.Gly141Ter
ENST00000545496.6:c.496G>T	ENSP00000441417.1:p.Gly166Ter
ENST00000672027.1:c.496G>T	ENSP00000500220.1:p.Gly166Ter
ENST00000672097.1:c.421G>T	ENSP00000500727.1:p.Gly141Ter
ENST00000672606.1:c.421G>T	ENSP00000500638.1:p.Gly141Ter
ENST00000672761.1:c.259G>T	ENSP00000500108.1:p.Gly87Ter
ENST00000673032.1:c.259G>T	ENSP00000500778.1:p.Gly87Ter
ENST00000381134.7:c.421G>T	ENSP00000370526.3:p.Gly141Ter
ENST00000438544.5:c.421G>T	ENSP00000406528.1:p.Gly141Ter
ENST00000483425.1:n.77G>T
ENST00000540563.5:c.286G>T	ENSP00000438198.1:p.Gly96Ter
ENST00000545496.5:c.496G>T	ENSP00000441417.1:p.Gly166Ter
NM_000047.2:c.421G>T	NP_000038.2:p.Gly141Ter
NM_001282628.1:c.496G>T	NP_001269557.1:p.Gly166Ter
NM_001282631.1:c.286G>T	NP_001269560.1:p.Gly96Ter
XM_005274518.2:c.448G>T	XP_005274575.1:p.Gly150Ter
XM_005274519.3:c.421G>T	XP_005274576.1:p.Gly141Ter
XM_005274521.3:c.259G>T	XP_005274578.1:p.Gly87Ter
XM_011545519.1:c.259G>T	XP_011543821.1:p.Gly87Ter
XM_011545520.1:c.496G>T	XP_011543822.1:p.Gly166Ter
XM_011545521.1:c.421G>T	XP_011543823.1:p.Gly141Ter
XM_005274519.4:c.421G>T	XP_005274576.1:p.Gly141Ter
XM_005274521.4:c.259G>T	XP_005274578.1:p.Gly87Ter
XM_017029525.1:c.496G>T	XP_016885014.1:p.Gly166Ter
XM_017029526.1:c.496G>T	XP_016885015.1:p.Gly166Ter
NM_000047.3:c.421G>T MANE Select	NP_000038.2:p.Gly141Ter
NM_001282631.2:c.259G>T	NP_001269560.2:p.Gly87Ter
NM_001369079.1:c.448G>T	NP_001356008.1:p.Gly150Ter
NM_001369080.1:c.496G>T	NP_001356009.1:p.Gly166Ter
NM_001282628.2:c.496G>T	NP_001269557.1:p.Gly166Ter