Canonical Allele Identifier: CA2412580499

Gene: ARSL

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.2934869G= , CM000685.2:g.2934869G=	GRCh38
NC_000023.10:g.2852910G= , CM000685.1:g.2852910G=	GRCh37
NC_000023.9:g.2862910G=	NCBI36
NG_007091.1:g.34402C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000540563.6:c.1733C=	ENSP00000438198.2:p.Pro578=
ENST00000681963.1:c.1808C=	ENSP00000507760.1:p.Pro603=
ENST00000682184.1:c.1610C=	ENSP00000507043.1:p.Pro537=
ENST00000682364.1:c.1172C=	ENSP00000507604.1:p.Pro391=
ENST00000683191.1:n.1513C=
ENST00000683290.1:c.1808C=	ENSP00000508156.1:p.Pro603=
ENST00000683677.1:c.1721C=	ENSP00000506786.1:p.Pro574=
ENST00000684077.1:c.1286C=	ENSP00000506767.1:p.Pro429=
ENST00000684117.1:c.1571C=	ENSP00000508337.1:p.Pro524=
ENST00000684364.1:c.1721C=	ENSP00000507304.1:p.Pro574=
ENST00000684738.1:c.1172C=	ENSP00000507481.1:p.Pro391=
ENST00000381134.9:c.1733C= MANE Select	ENSP00000370526.3:p.Pro578=
ENST00000545496.6:c.1808C=	ENSP00000441417.1:p.Pro603=
ENST00000672027.1:c.1808C=	ENSP00000500220.1:p.Pro603=
ENST00000672097.1:c.1730C=	ENSP00000500727.1:p.Pro577=
ENST00000672761.1:c.1571C=	ENSP00000500108.1:p.Pro524=
ENST00000673032.1:c.1571C=	ENSP00000500778.1:p.Pro524=
ENST00000381134.7:c.1733C=	ENSP00000370526.3:p.Pro578=
ENST00000540563.5:c.1598C=	ENSP00000438198.1:p.Pro533=
ENST00000545496.5:c.1808C=	ENSP00000441417.1:p.Pro603=
NM_000047.2:c.1733C=	NP_000038.2:p.Pro578=
NM_001282628.1:c.1808C=	NP_001269557.1:p.Pro603=
NM_001282631.1:c.1598C=	NP_001269560.1:p.Pro533=
XM_005274518.2:c.1760C=	XP_005274575.1:p.Pro587=
XM_005274519.3:c.1733C=	XP_005274576.1:p.Pro578=
XM_005274521.3:c.1571C=	XP_005274578.1:p.Pro524=
XM_011545519.1:c.1571C=	XP_011543821.1:p.Pro524=
XM_011545520.1:c.1247C=	XP_011543822.1:p.Pro416=
XM_011545521.1:c.1172C=	XP_011543823.1:p.Pro391=
XM_005274519.4:c.1733C=	XP_005274576.1:p.Pro578=
XM_005274521.4:c.1571C=	XP_005274578.1:p.Pro524=
XM_017029525.1:c.1808C=	XP_016885014.1:p.Pro603=
XM_017029526.1:c.1247C=	XP_016885015.1:p.Pro416=
NM_000047.3:c.1733C= MANE Select	NP_000038.2:p.Pro578=
NM_001282631.2:c.1571C=	NP_001269560.2:p.Pro524=
NM_001369079.1:c.1760C=	NP_001356008.1:p.Pro587=
NM_001369080.1:c.1808C=	NP_001356009.1:p.Pro603=
NM_001282628.2:c.1808C=	NP_001269557.1:p.Pro603=