Canonical Allele Identifier: CA2499754049

Gene: XYLB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38401162_38401163insTGGGATTTGG , CM000665.2:g.38401162_38401163insTGGGATTTGG	GRCh38
NC_000003.11:g.38442653_38442654insTGGGATTTGG , CM000665.1:g.38442653_38442654insTGGGATTTGG	GRCh37
NC_000003.10:g.38417657_38417658insTGGGATTTGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000207870.8:c.1533+177_1533+178insTGGGATTTGG MANE Select	ENSP00000207870.3:n.1533+177_1533+178insTGGGATTTGG
ENST00000649234.1:c.*768+177_*768+178insTGGGATTTGG	ENSP00000497023.1:n.*768+177_*768+178insTGGGATTTGG
ENST00000650590.1:c.1452+177_1452+178insTGGGATTTGG	ENSP00000496840.1:n.1452+177_1452+178insTGGGATTTGG
ENST00000207870.7:c.1533+177_1533+178insTGGGATTTGG	ENSP00000207870.3:n.1533+177_1533+178insTGGGATTTGG
ENST00000424034.5:c.*1196+177_*1196+178insTGGGATTTGG	ENSP00000398845.1:n.*1196+177_*1196+178insTGGGATTTGG
ENST00000472721.1:n.410+177_410+178insTGGGATTTGG
NM_005108.3:c.1533+177_1533+178insTGGGATTTGG	NP_005099.2:n.1533+177_1533+178insTGGGATTTGG
XM_011534325.1:c.1533+177_1533+178insTGGGATTTGG	XP_011532627.1:n.1533+177_1533+178insTGGGATTTGG
XM_011534326.1:c.1452+177_1452+178insTGGGATTTGG	XP_011532628.1:n.1452+177_1452+178insTGGGATTTGG
XM_011534327.1:c.1533+177_1533+178insTGGGATTTGG	XP_011532629.1:n.1533+177_1533+178insTGGGATTTGG
XM_011534328.1:c.1533+177_1533+178insTGGGATTTGG	XP_011532630.1:n.1533+177_1533+178insTGGGATTTGG
XM_011534329.1:c.1533+177_1533+178insTGGGATTTGG	XP_011532631.1:n.1533+177_1533+178insTGGGATTTGG
XM_011534330.1:c.1533+177_1533+178insTGGGATTTGG	XP_011532632.1:n.1533+177_1533+178insTGGGATTTGG
NM_001349178.1:c.1533+177_1533+178insTGGGATTTGG	NP_001336107.1:n.1533+177_1533+178insTGGGATTTGG
NM_001349179.1:c.1122+177_1122+178insTGGGATTTGG	NP_001336108.1:n.1122+177_1122+178insTGGGATTTGG
NR_146068.1:n.1450+177_1450+178insTGGGATTTGG
XM_011534325.3:c.1533+177_1533+178insTGGGATTTGG	XP_011532627.1:n.1533+177_1533+178insTGGGATTTGG
XM_011534327.2:c.1533+177_1533+178insTGGGATTTGG	XP_011532629.1:n.1533+177_1533+178insTGGGATTTGG
XM_011534328.3:c.1533+177_1533+178insTGGGATTTGG	XP_011532630.1:n.1533+177_1533+178insTGGGATTTGG
XM_011534329.2:c.1533+177_1533+178insTGGGATTTGG	XP_011532631.1:n.1533+177_1533+178insTGGGATTTGG
XM_011534330.3:c.1533+177_1533+178insTGGGATTTGG	XP_011532632.1:n.1533+177_1533+178insTGGGATTTGG
XM_017007595.1:c.1122+177_1122+178insTGGGATTTGG	XP_016863084.1:n.1122+177_1122+178insTGGGATTTGG
XM_017007596.1:c.1335+177_1335+178insTGGGATTTGG	XP_016863085.1:n.1335+177_1335+178insTGGGATTTGG
XM_017007597.1:c.852+177_852+178insTGGGATTTGG	XP_016863086.1:n.852+177_852+178insTGGGATTTGG
XM_024453850.1:c.1335+177_1335+178insTGGGATTTGG	XP_024309618.1:n.1335+177_1335+178insTGGGATTTGG
NM_001349178.2:c.1533+177_1533+178insTGGGATTTGG	NP_001336107.1:n.1533+177_1533+178insTGGGATTTGG
NM_005108.4:c.1533+177_1533+178insTGGGATTTGG MANE Select	NP_005099.2:n.1533+177_1533+178insTGGGATTTGG
NR_146068.2:n.1425+177_1425+178insTGGGATTTGG
NM_001349179.2:c.1122+177_1122+178insTGGGATTTGG	NP_001336108.1:n.1122+177_1122+178insTGGGATTTGG