Canonical Allele Identifier: CA2631987622

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17138721-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138724del , CM000678.2:g.17138724del	GRCh38
NC_000016.9:g.17232581del , CM000678.1:g.17232581del	GRCh37
NC_000016.8:g.17140082del	NCBI36
NG_015843.1:g.337160del
NG_015843.2:g.337160del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-191del MANE Select	ENSP00000261381.6:n.1588-191del
ENST00000261381.6:c.1588-191del	ENSP00000261381.6:n.1588-191del
NM_022166.3:c.1588-191del	NP_071449.1:n.1588-191del
XM_011522574.1:c.1588-191del	XP_011520876.1:n.1588-191del
XR_933141.1:n.657del
NR_135179.1:n.629del
XM_017023539.2:c.1588-191del	XP_016879028.1:n.1588-191del
XM_017023540.2:c.1588-191del	XP_016879029.1:n.1588-191del
NM_022166.4:c.1588-191del MANE Select	NP_071449.1:n.1588-191del