Canonical Allele Identifier: CA412275445

Gene: ARSL

Linked Data

• gnomAD v4: X-2935007-G-T
• MyVariant Identifiers: chrX:g.2853048G>T (hg19) ; chrX:g.2935007G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.2935007G>T , CM000685.2:g.2935007G>T	GRCh38
NC_000023.10:g.2853048G>T , CM000685.1:g.2853048G>T	GRCh37
NC_000023.9:g.2863048G>T	NCBI36
NG_007091.1:g.34264C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540563.6:c.1595C>A	ENSP00000438198.2:p.Pro532His
ENST00000681963.1:c.1670C>A	ENSP00000507760.1:p.Pro557His
ENST00000682184.1:c.1472C>A	ENSP00000507043.1:p.Pro491His
ENST00000682364.1:c.1034C>A	ENSP00000507604.1:p.Pro345His
ENST00000683191.1:n.1375C>A
ENST00000683290.1:c.1670C>A	ENSP00000508156.1:p.Pro557His
ENST00000683677.1:c.1583C>A	ENSP00000506786.1:p.Pro528His
ENST00000684077.1:c.1148C>A	ENSP00000506767.1:p.Pro383His
ENST00000684117.1:c.1433C>A	ENSP00000508337.1:p.Pro478His
ENST00000684364.1:c.1583C>A	ENSP00000507304.1:p.Pro528His
ENST00000684738.1:c.1034C>A	ENSP00000507481.1:p.Pro345His
ENST00000381134.9:c.1595C>A MANE Select	ENSP00000370526.3:p.Pro532His
ENST00000545496.6:c.1670C>A	ENSP00000441417.1:p.Pro557His
ENST00000672027.1:c.1670C>A	ENSP00000500220.1:p.Pro557His
ENST00000672097.1:c.1592C>A	ENSP00000500727.1:p.Pro531His
ENST00000672761.1:c.1433C>A	ENSP00000500108.1:p.Pro478His
ENST00000673032.1:c.1433C>A	ENSP00000500778.1:p.Pro478His
ENST00000381134.7:c.1595C>A	ENSP00000370526.3:p.Pro532His
ENST00000540563.5:c.1460C>A	ENSP00000438198.1:p.Pro487His
ENST00000545496.5:c.1670C>A	ENSP00000441417.1:p.Pro557His
NM_000047.2:c.1595C>A	NP_000038.2:p.Pro532His
NM_001282628.1:c.1670C>A	NP_001269557.1:p.Pro557His
NM_001282631.1:c.1460C>A	NP_001269560.1:p.Pro487His
XM_005274518.2:c.1622C>A	XP_005274575.1:p.Pro541His
XM_005274519.3:c.1595C>A	XP_005274576.1:p.Pro532His
XM_005274521.3:c.1433C>A	XP_005274578.1:p.Pro478His
XM_011545519.1:c.1433C>A	XP_011543821.1:p.Pro478His
XM_011545520.1:c.1109C>A	XP_011543822.1:p.Pro370His
XM_011545521.1:c.1034C>A	XP_011543823.1:p.Pro345His
XM_005274519.4:c.1595C>A	XP_005274576.1:p.Pro532His
XM_005274521.4:c.1433C>A	XP_005274578.1:p.Pro478His
XM_017029525.1:c.1670C>A	XP_016885014.1:p.Pro557His
XM_017029526.1:c.1109C>A	XP_016885015.1:p.Pro370His
NM_000047.3:c.1595C>A MANE Select	NP_000038.2:p.Pro532His
NM_001282631.2:c.1433C>A	NP_001269560.2:p.Pro478His
NM_001369079.1:c.1622C>A	NP_001356008.1:p.Pro541His
NM_001369080.1:c.1670C>A	NP_001356009.1:p.Pro557His
NM_001282628.2:c.1670C>A	NP_001269557.1:p.Pro557His