Canonical Allele Identifier: CA2210538837

Gene: XYLT1

Linked Data

• dbSNP Id: rs2030644880

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17134745_17134753dup , CM000678.2:g.17134745_17134753dup	GRCh38
NC_000016.9:g.17228602_17228610dup , CM000678.1:g.17228602_17228610dup	GRCh37
NC_000016.8:g.17136103_17136111dup	NCBI36
NG_015843.1:g.341130_341138dup
NG_015843.2:g.341130_341138dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1765-17_1765-9dup MANE Select	ENSP00000261381.6:n.1765-17_1765-9dup
ENST00000261381.6:c.1765-17_1765-9dup	ENSP00000261381.6:n.1765-17_1765-9dup
NM_022166.3:c.1765-17_1765-9dup	NP_071449.1:n.1765-17_1765-9dup
XM_011522574.1:c.1765-17_1765-9dup	XP_011520876.1:n.1765-17_1765-9dup
XR_933140.1:n.82+195_82+203dup
XR_933141.1:n.75+195_75+203dup
XR_933143.1:n.82+195_82+203dup
NR_135179.1:n.47+195_47+203dup
XM_017023539.2:c.1765-17_1765-9dup	XP_016879028.1:n.1765-17_1765-9dup
XM_017023540.2:c.1765-17_1765-9dup	XP_016879029.1:n.1765-17_1765-9dup
NM_022166.4:c.1765-17_1765-9dup MANE Select	NP_071449.1:n.1765-17_1765-9dup