Canonical Allele Identifier: CA2210542417

Gene: XYLT1

Linked Data

• dbSNP Id: rs2030859201
• gnomAD v4: 16-17138626-T-TAAGA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138628_17138631dup , CM000678.2:g.17138628_17138631dup	GRCh38
NC_000016.9:g.17232485_17232488dup , CM000678.1:g.17232485_17232488dup	GRCh37
NC_000016.8:g.17139986_17139989dup	NCBI36
NG_015843.1:g.337252_337255dup
NG_015843.2:g.337252_337255dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-99_1588-96dup MANE Select	ENSP00000261381.6:n.1588-99_1588-96dup
ENST00000261381.6:c.1588-99_1588-96dup	ENSP00000261381.6:n.1588-99_1588-96dup
NM_022166.3:c.1588-99_1588-96dup	NP_071449.1:n.1588-99_1588-96dup
XM_011522574.1:c.1588-99_1588-96dup	XP_011520876.1:n.1588-99_1588-96dup
XR_933141.1:n.561_564dup
NR_135179.1:n.533_536dup
XM_017023539.2:c.1588-99_1588-96dup	XP_016879028.1:n.1588-99_1588-96dup
XM_017023540.2:c.1588-99_1588-96dup	XP_016879029.1:n.1588-99_1588-96dup
NM_022166.4:c.1588-99_1588-96dup MANE Select	NP_071449.1:n.1588-99_1588-96dup