Canonical Allele Identifier: CA360338602

Gene: ARSB

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.78839356A>T , CM000667.2:g.78839356A>T	GRCh38
NC_000005.9:g.78135179A>T , CM000667.1:g.78135179A>T	GRCh37
NC_000005.8:g.78170935A>T	NCBI36
NG_007089.1:g.152179T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264914.10:c.1213T>A MANE Select	ENSP00000264914.4:p.Cys405Ser
ENST00000264914.8:c.1213T>A	ENSP00000264914.4:p.Cys405Ser
ENST00000396151.7:c.1213T>A	ENSP00000379455.3:p.Tyr405Asn
ENST00000565165.1:c.1213T>A	ENSP00000456339.1:p.Tyr405Asn
NM_000046.3:c.1213T>A	NP_000037.2:p.Cys405Ser
NM_198709.2:c.1213T>A	NP_942002.1:p.Tyr405Asn
XM_005248506.3:c.1213T>A	XP_005248563.1:p.Ter405Lys
XM_011543390.1:c.1213T>A	XP_011541692.1:p.Cys405Ser
XM_011543391.1:c.1213T>A	XP_011541693.1:p.Ser405Thr
XM_011543392.1:c.1213T>A	XP_011541694.1:p.Trp405Arg
NM_000046.4:c.1213T>A	NP_000037.2:p.Cys405Ser
XM_011543391.3:c.1213T>A	XP_011541693.1:p.Ser405Thr
XM_011543392.3:c.1213T>A	XP_011541694.1:p.Trp405Arg
XM_017009471.2:c.1213T>A	XP_016864960.1:p.Cys405Ser
XR_001742065.2:n.1284T>A
XR_001742066.2:n.1284T>A
NM_000046.5:c.1213T>A MANE Select	NP_000037.2:p.Cys405Ser
NM_198709.3:c.1213T>A	NP_942002.1:p.Tyr405Asn