Canonical Allele Identifier: CA412268778

Gene: ARSL

Linked Data

• MyVariant Identifiers: chrX:g.2876464C>A (hg19) ; chrX:g.2958423C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.2958423C>A , CM000685.2:g.2958423C>A	GRCh38
NC_000023.10:g.2876464C>A , CM000685.1:g.2876464C>A	GRCh37
NC_000023.9:g.2886464C>A	NCBI36
NG_007091.1:g.10848G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483425.2:n.121G>T
ENST00000540563.6:c.36G>T	ENSP00000438198.2:p.Arg12Ser
ENST00000681960.1:n.362G>T
ENST00000681963.1:c.111G>T	ENSP00000507760.1:p.Arg37Ser
ENST00000682184.1:c.36G>T	ENSP00000507043.1:p.Arg12Ser
ENST00000682364.1:c.36G>T	ENSP00000507604.1:p.Arg12Ser
ENST00000682745.1:n.121G>T
ENST00000683071.1:n.77+1955G>T
ENST00000683290.1:c.111G>T	ENSP00000508156.1:p.Arg37Ser
ENST00000683677.1:c.24G>T	ENSP00000506786.1:p.Trp8Cys
ENST00000683854.1:n.121G>T
ENST00000683958.1:c.36G>T	ENSP00000507756.1:p.Arg12Ser
ENST00000684045.1:n.350G>T
ENST00000684077.1:c.23+1955G>T	ENSP00000506767.1:n.23+1955G>T
ENST00000684117.1:c.23+1955G>T	ENSP00000508337.1:n.23+1955G>T
ENST00000684364.1:c.24G>T	ENSP00000507304.1:p.Trp8Cys
ENST00000684687.1:c.23+1955G>T	ENSP00000507266.1:n.23+1955G>T
ENST00000684738.1:c.36G>T	ENSP00000507481.1:p.Arg12Ser
ENST00000381134.9:c.36G>T MANE Select	ENSP00000370526.3:p.Arg12Ser
ENST00000545496.6:c.111G>T	ENSP00000441417.1:p.Arg37Ser
ENST00000672027.1:c.111G>T	ENSP00000500220.1:p.Arg37Ser
ENST00000672097.1:c.36G>T	ENSP00000500727.1:p.Arg12Ser
ENST00000672606.1:c.36G>T	ENSP00000500638.1:p.Arg12Ser
ENST00000672761.1:c.23+1955G>T	ENSP00000500108.1:n.23+1955G>T
ENST00000673032.1:c.23+1955G>T	ENSP00000500778.1:n.23+1955G>T
ENST00000381134.7:c.36G>T	ENSP00000370526.3:p.Arg12Ser
ENST00000438544.5:c.36G>T	ENSP00000406528.1:p.Arg12Ser
ENST00000496095.1:n.383G>T
ENST00000540563.5:c.50+1955G>T	ENSP00000438198.1:n.50+1955G>T
ENST00000545496.5:c.111G>T	ENSP00000441417.1:p.Arg37Ser
NM_000047.2:c.36G>T	NP_000038.2:p.Arg12Ser
NM_001282628.1:c.111G>T	NP_001269557.1:p.Arg37Ser
NM_001282631.1:c.50+1955G>T	NP_001269560.1:n.50+1955G>T
XM_005274518.2:c.63G>T	XP_005274575.1:p.Arg21Ser
XM_005274519.3:c.36G>T	XP_005274576.1:p.Arg12Ser
XM_005274521.3:c.23+1955G>T	XP_005274578.1:n.23+1955G>T
XM_011545519.1:c.23+1955G>T	XP_011543821.1:n.23+1955G>T
XM_011545520.1:c.111G>T	XP_011543822.1:p.Arg37Ser
XM_011545521.1:c.36G>T	XP_011543823.1:p.Arg12Ser
XM_005274519.4:c.36G>T	XP_005274576.1:p.Arg12Ser
XM_005274521.4:c.23+1955G>T	XP_005274578.1:n.23+1955G>T
XM_017029525.1:c.111G>T	XP_016885014.1:p.Arg37Ser
XM_017029526.1:c.111G>T	XP_016885015.1:p.Arg37Ser
NM_000047.3:c.36G>T MANE Select	NP_000038.2:p.Arg12Ser
NM_001282631.2:c.23+1955G>T	NP_001269560.2:n.23+1955G>T
NM_001369079.1:c.63G>T	NP_001356008.1:p.Arg21Ser
NM_001369080.1:c.111G>T	NP_001356009.1:p.Arg37Ser
NM_001282628.2:c.111G>T	NP_001269557.1:p.Arg37Ser