Canonical Allele Identifier: CA2210542800

Gene: XYLT1

Linked Data

• dbSNP Id: rs2030870390
• gnomAD v4: 16-17138828-T-TCAGCTGCCCATGTGGTC

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138831_17138847dup , CM000678.2:g.17138831_17138847dup	GRCh38
NC_000016.9:g.17232688_17232704dup , CM000678.1:g.17232688_17232704dup	GRCh37
NC_000016.8:g.17140189_17140205dup	NCBI36
NG_015843.1:g.337037_337053dup
NG_015843.2:g.337037_337053dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-314_1588-298dup MANE Select	ENSP00000261381.6:n.1588-314_1588-298dup
ENST00000261381.6:c.1588-314_1588-298dup	ENSP00000261381.6:n.1588-314_1588-298dup
NM_022166.3:c.1588-314_1588-298dup	NP_071449.1:n.1588-314_1588-298dup
XM_011522574.1:c.1588-314_1588-298dup	XP_011520876.1:n.1588-314_1588-298dup
XM_017023539.2:c.1588-314_1588-298dup	XP_016879028.1:n.1588-314_1588-298dup
XM_017023540.2:c.1588-314_1588-298dup	XP_016879029.1:n.1588-314_1588-298dup
NM_022166.4:c.1588-314_1588-298dup MANE Select	NP_071449.1:n.1588-314_1588-298dup