Canonical Allele Identifier: CA1358492413

Gene: XYLB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38401052_38401053delinsAC , CM000665.2:g.38401052_38401053delinsAC	GRCh38
NC_000003.11:g.38442543_38442544delinsAC , CM000665.1:g.38442543_38442544delinsAC	GRCh37
NC_000003.10:g.38417547_38417548delinsAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000207870.8:c.1533+67_1533+68delinsAC MANE Select	ENSP00000207870.3:n.1533+67_1533+68delinsAC
ENST00000649234.1:c.*768+67_*768+68delinsAC	ENSP00000497023.1:n.*768+67_*768+68delinsAC
ENST00000650590.1:c.1452+67_1452+68delinsAC	ENSP00000496840.1:n.1452+67_1452+68delinsAC
ENST00000207870.7:c.1533+67_1533+68delinsAC	ENSP00000207870.3:n.1533+67_1533+68delinsAC
ENST00000424034.5:c.*1196+67_*1196+68delinsAC	ENSP00000398845.1:n.*1196+67_*1196+68delinsAC
ENST00000472721.1:n.410+67_410+68delinsAC
NM_005108.3:c.1533+67_1533+68delinsAC	NP_005099.2:n.1533+67_1533+68delinsAC
XM_011534325.1:c.1533+67_1533+68delinsAC	XP_011532627.1:n.1533+67_1533+68delinsAC
XM_011534326.1:c.1452+67_1452+68delinsAC	XP_011532628.1:n.1452+67_1452+68delinsAC
XM_011534327.1:c.1533+67_1533+68delinsAC	XP_011532629.1:n.1533+67_1533+68delinsAC
XM_011534328.1:c.1533+67_1533+68delinsAC	XP_011532630.1:n.1533+67_1533+68delinsAC
XM_011534329.1:c.1533+67_1533+68delinsAC	XP_011532631.1:n.1533+67_1533+68delinsAC
XM_011534330.1:c.1533+67_1533+68delinsAC	XP_011532632.1:n.1533+67_1533+68delinsAC
NM_001349178.1:c.1533+67_1533+68delinsAC	NP_001336107.1:n.1533+67_1533+68delinsAC
NM_001349179.1:c.1122+67_1122+68delinsAC	NP_001336108.1:n.1122+67_1122+68delinsAC
NR_146068.1:n.1450+67_1450+68delinsAC
XM_011534325.3:c.1533+67_1533+68delinsAC	XP_011532627.1:n.1533+67_1533+68delinsAC
XM_011534327.2:c.1533+67_1533+68delinsAC	XP_011532629.1:n.1533+67_1533+68delinsAC
XM_011534328.3:c.1533+67_1533+68delinsAC	XP_011532630.1:n.1533+67_1533+68delinsAC
XM_011534329.2:c.1533+67_1533+68delinsAC	XP_011532631.1:n.1533+67_1533+68delinsAC
XM_011534330.3:c.1533+67_1533+68delinsAC	XP_011532632.1:n.1533+67_1533+68delinsAC
XM_017007595.1:c.1122+67_1122+68delinsAC	XP_016863084.1:n.1122+67_1122+68delinsAC
XM_017007596.1:c.1335+67_1335+68delinsAC	XP_016863085.1:n.1335+67_1335+68delinsAC
XM_017007597.1:c.852+67_852+68delinsAC	XP_016863086.1:n.852+67_852+68delinsAC
XM_024453850.1:c.1335+67_1335+68delinsAC	XP_024309618.1:n.1335+67_1335+68delinsAC
NM_001349178.2:c.1533+67_1533+68delinsAC	NP_001336107.1:n.1533+67_1533+68delinsAC
NM_005108.4:c.1533+67_1533+68delinsAC MANE Select	NP_005099.2:n.1533+67_1533+68delinsAC
NR_146068.2:n.1425+67_1425+68delinsAC
NM_001349179.2:c.1122+67_1122+68delinsAC	NP_001336108.1:n.1122+67_1122+68delinsAC