Canonical Allele Identifier: CA1557701729

Gene: ARSB

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.78964443G= , CM000667.2:g.78964443G=	GRCh38
NC_000005.9:g.78260266G= , CM000667.1:g.78260266G=	GRCh37
NC_000005.8:g.78296022G=	NCBI36
NG_007089.1:g.27092C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264914.10:c.663C= MANE Select	ENSP00000264914.4:p.Ala221=
ENST00000565165.2:c.663C=	ENSP00000456339.2:p.Ala221=
ENST00000264914.8:c.663C=	ENSP00000264914.4:p.Ala221=
ENST00000396151.7:c.663C=	ENSP00000379455.3:p.Ala221=
ENST00000565165.1:c.663C=	ENSP00000456339.1:p.Ala221=
NM_000046.3:c.663C=	NP_000037.2:p.Ala221=
NM_198709.2:c.663C=	NP_942002.1:p.Ala221=
XM_005248506.3:c.663C=	XP_005248563.1:p.Ala221=
XM_006714615.2:c.663C=	XP_006714678.1:p.Ala221=
XM_011543390.1:c.663C=	XP_011541692.1:p.Ala221=
XM_011543391.1:c.663C=	XP_011541693.1:p.Ala221=
XM_011543392.1:c.663C=	XP_011541694.1:p.Ala221=
XM_011543393.1:c.663C=	XP_011541695.1:p.Ala221=
NM_000046.4:c.663C=	NP_000037.2:p.Ala221=
XM_011543391.3:c.663C=	XP_011541693.1:p.Ala221=
XM_011543392.3:c.663C=	XP_011541694.1:p.Ala221=
XM_011543393.2:c.663C=	XP_011541695.1:p.Ala221=
XM_017009471.2:c.663C=	XP_016864960.1:p.Ala221=
XR_001742065.2:n.734C=
XR_001742066.2:n.734C=
NM_000046.5:c.663C= MANE Select	NP_000037.2:p.Ala221=
NM_198709.3:c.663C=	NP_942002.1:p.Ala221=