Canonical Allele Identifier: CA2741470686

Gene: XYLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17134756_17134758dup , CM000678.2:g.17134756_17134758dup	GRCh38
NC_000016.9:g.17228613_17228615dup , CM000678.1:g.17228613_17228615dup	GRCh37
NC_000016.8:g.17136114_17136116dup	NCBI36
NG_015843.1:g.341125_341127dup
NG_015843.2:g.341125_341127dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1765-22_1765-20dup MANE Select	ENSP00000261381.6:n.1765-22_1765-20dup
ENST00000261381.6:c.1765-22_1765-20dup	ENSP00000261381.6:n.1765-22_1765-20dup
NM_022166.3:c.1765-22_1765-20dup	NP_071449.1:n.1765-22_1765-20dup
XM_011522574.1:c.1765-22_1765-20dup	XP_011520876.1:n.1765-22_1765-20dup
XR_933140.1:n.82+206_82+208dup
XR_933141.1:n.75+206_75+208dup
XR_933143.1:n.82+206_82+208dup
NR_135179.1:n.47+206_47+208dup
XM_017023539.2:c.1765-22_1765-20dup	XP_016879028.1:n.1765-22_1765-20dup
XM_017023540.2:c.1765-22_1765-20dup	XP_016879029.1:n.1765-22_1765-20dup
NM_022166.4:c.1765-22_1765-20dup MANE Select	NP_071449.1:n.1765-22_1765-20dup