Canonical Allele Identifier: CA2631987618

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17138705-C-CAAATAAACCTCTTTTCTTTATAA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138707_17138729dup , CM000678.2:g.17138707_17138729dup	GRCh38
NC_000016.9:g.17232564_17232586dup , CM000678.1:g.17232564_17232586dup	GRCh37
NC_000016.8:g.17140065_17140087dup	NCBI36
NG_015843.1:g.337154_337176dup
NG_015843.2:g.337154_337176dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-197_1588-175dup MANE Select	ENSP00000261381.6:n.1588-197_1588-175dup
ENST00000261381.6:c.1588-197_1588-175dup	ENSP00000261381.6:n.1588-197_1588-175dup
NM_022166.3:c.1588-197_1588-175dup	NP_071449.1:n.1588-197_1588-175dup
XM_011522574.1:c.1588-197_1588-175dup	XP_011520876.1:n.1588-197_1588-175dup
XR_933141.1:n.640_662dup
NR_135179.1:n.612_634dup
XM_017023539.2:c.1588-197_1588-175dup	XP_016879028.1:n.1588-197_1588-175dup
XM_017023540.2:c.1588-197_1588-175dup	XP_016879029.1:n.1588-197_1588-175dup
NM_022166.4:c.1588-197_1588-175dup MANE Select	NP_071449.1:n.1588-197_1588-175dup