Canonical Allele Identifier: CA352127202

Gene: XYLB

Linked Data

• dbSNP Id: rs1451757694
• MyVariant Identifiers: chr3:g.38442400A>T (hg19) ; chr3:g.38400909A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38400909A>T , CM000665.2:g.38400909A>T	GRCh38
NC_000003.11:g.38442400A>T , CM000665.1:g.38442400A>T	GRCh37
NC_000003.10:g.38417404A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000207870.8:c.1457A>T MANE Select	ENSP00000207870.3:p.Asp486Val
ENST00000649234.1:c.*692A>T	ENSP00000497023.1:n.*692A>T
ENST00000650590.1:c.1376A>T	ENSP00000496840.1:p.Asp459Val
ENST00000207870.7:c.1457A>T	ENSP00000207870.3:p.Asp486Val
ENST00000424034.5:c.*1120A>T	ENSP00000398845.1:n.*1120A>T
ENST00000472721.1:n.334A>T
NM_005108.3:c.1457A>T	NP_005099.2:p.Asp486Val
XM_011534325.1:c.1457A>T	XP_011532627.1:p.Asp486Val
XM_011534326.1:c.1376A>T	XP_011532628.1:p.Asp459Val
XM_011534327.1:c.1457A>T	XP_011532629.1:p.Asp486Val
XM_011534328.1:c.1457A>T	XP_011532630.1:p.Asp486Val
XM_011534329.1:c.1457A>T	XP_011532631.1:p.Asp486Val
XM_011534330.1:c.1457A>T	XP_011532632.1:p.Asp486Val
NM_001349178.1:c.1457A>T	NP_001336107.1:p.Asp486Val
NM_001349179.1:c.1046A>T	NP_001336108.1:p.Asp349Val
NR_146068.1:n.1374A>T
XM_011534325.3:c.1457A>T	XP_011532627.1:p.Asp486Val
XM_011534327.2:c.1457A>T	XP_011532629.1:p.Asp486Val
XM_011534328.3:c.1457A>T	XP_011532630.1:p.Asp486Val
XM_011534329.2:c.1457A>T	XP_011532631.1:p.Asp486Val
XM_011534330.3:c.1457A>T	XP_011532632.1:p.Asp486Val
XM_017007595.1:c.1046A>T	XP_016863084.1:p.Asp349Val
XM_017007596.1:c.1259A>T	XP_016863085.1:p.Asp420Val
XM_017007597.1:c.776A>T	XP_016863086.1:p.Asp259Val
XM_017007599.2:c.*67A>T	XP_016863088.1:n.*67A>T
XM_024453850.1:c.1259A>T	XP_024309618.1:p.Asp420Val
NM_001349178.2:c.1457A>T	NP_001336107.1:p.Asp486Val
NM_005108.4:c.1457A>T MANE Select	NP_005099.2:p.Asp486Val
NR_146068.2:n.1349A>T
NM_001349179.2:c.1046A>T	NP_001336108.1:p.Asp349Val