Canonical Allele Identifier: CA7927846

Gene: XYLT1

Linked Data

• ClinVar Variation Id: 2716664
• ClinVar RCV Id: RCV003496540
• dbSNP Id: rs772084738
• ExAC: 16:17232397 G / A
• gnomAD v2: 16-17232397-G-A
• gnomAD v3: 16-17138540-G-A
• gnomAD v4: 16-17138540-G-A
• MyVariant Identifiers: chr16:g.17232397G>A (hg19) ; chr16:g.17138540G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138540G>A , CM000678.2:g.17138540G>A	GRCh38
NC_000016.9:g.17232397G>A , CM000678.1:g.17232397G>A	GRCh37
NC_000016.8:g.17139898G>A	NCBI36
NG_015843.1:g.337342C>T
NG_015843.2:g.337342C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261381.7:c.1588-9C>T MANE Select	ENSP00000261381.6:n.1588-9C>T
ENST00000261381.6:c.1588-9C>T	ENSP00000261381.6:n.1588-9C>T
NM_022166.3:c.1588-9C>T	NP_071449.1:n.1588-9C>T
XM_011522574.1:c.1588-9C>T	XP_011520876.1:n.1588-9C>T
XR_933141.1:n.473G>A
NR_135179.1:n.445G>A
XM_017023539.2:c.1588-9C>T	XP_016879028.1:n.1588-9C>T
XM_017023540.2:c.1588-9C>T	XP_016879029.1:n.1588-9C>T
NM_022166.4:c.1588-9C>T MANE Select	NP_071449.1:n.1588-9C>T