Canonical Allele Identifier: CA2210541744

Gene: XYLT1

Linked Data

• dbSNP Id: rs2030836503
• gnomAD v4: 16-17138325-G-GGAGGCTGGCAGACCATGA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138328_17138345dup , CM000678.2:g.17138328_17138345dup	GRCh38
NC_000016.9:g.17232185_17232202dup , CM000678.1:g.17232185_17232202dup	GRCh37
NC_000016.8:g.17139686_17139703dup	NCBI36
NG_015843.1:g.337539_337556dup
NG_015843.2:g.337539_337556dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+12_1764+29dup MANE Select	ENSP00000261381.6:n.1764+12_1764+29dup
ENST00000261381.6:c.1764+12_1764+29dup	ENSP00000261381.6:n.1764+12_1764+29dup
NM_022166.3:c.1764+12_1764+29dup	NP_071449.1:n.1764+12_1764+29dup
XM_011522574.1:c.1764+12_1764+29dup	XP_011520876.1:n.1764+12_1764+29dup
XR_933140.1:n.422_439dup
XR_933141.1:n.261_278dup
XR_933143.1:n.323_340dup
NR_135179.1:n.233_250dup
XM_017023539.2:c.1764+12_1764+29dup	XP_016879028.1:n.1764+12_1764+29dup
XM_017023540.2:c.1764+12_1764+29dup	XP_016879029.1:n.1764+12_1764+29dup
NM_022166.4:c.1764+12_1764+29dup MANE Select	NP_071449.1:n.1764+12_1764+29dup