Canonical Allele Identifier: CA360342862

Gene: ARSB

Linked Data

• MyVariant Identifiers: chr5:g.78181486G>A (hg19) ; chr5:g.78885663G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.78885663G>A , CM000667.2:g.78885663G>A	GRCh38
NC_000005.9:g.78181486G>A , CM000667.1:g.78181486G>A	GRCh37
NC_000005.8:g.78217242G>A	NCBI36
NG_007089.1:g.105872C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264914.10:c.1063C>T MANE Select	ENSP00000264914.4:p.Pro355Ser
ENST00000521800.2:n.245C>T
ENST00000565165.2:c.1063C>T	ENSP00000456339.2:p.Pro355Ser
ENST00000264914.8:c.1063C>T	ENSP00000264914.4:p.Pro355Ser
ENST00000396151.7:c.1063C>T	ENSP00000379455.3:p.Pro355Ser
ENST00000521800.1:n.168C>T
ENST00000565165.1:c.1063C>T	ENSP00000456339.1:p.Pro355Ser
NM_000046.3:c.1063C>T	NP_000037.2:p.Pro355Ser
NM_198709.2:c.1063C>T	NP_942002.1:p.Pro355Ser
XM_005248506.3:c.1063C>T	XP_005248563.1:p.Pro355Ser
XM_011543390.1:c.1063C>T	XP_011541692.1:p.Pro355Ser
XM_011543391.1:c.1063C>T	XP_011541693.1:p.Pro355Ser
XM_011543392.1:c.1063C>T	XP_011541694.1:p.Pro355Ser
XM_011543393.1:c.1063C>T	XP_011541695.1:p.Pro355Ser
NM_000046.4:c.1063C>T	NP_000037.2:p.Pro355Ser
XM_011543391.3:c.1063C>T	XP_011541693.1:p.Pro355Ser
XM_011543392.3:c.1063C>T	XP_011541694.1:p.Pro355Ser
XM_011543393.2:c.1063C>T	XP_011541695.1:p.Pro355Ser
XM_017009471.2:c.1063C>T	XP_016864960.1:p.Pro355Ser
XR_001742065.2:n.1134C>T
XR_001742066.2:n.1134C>T
NM_000046.5:c.1063C>T MANE Select	NP_000037.2:p.Pro355Ser
NM_198709.3:c.1063C>T	NP_942002.1:p.Pro355Ser