Canonical Allele Identifier: CA278644226

Gene: XYLT1

Linked Data

• dbSNP Id: rs1555481563
• gnomAD v4: 16-17138147-G-GTTAATGAGTCAATGTGGT
• MyVariant Identifiers: chr16:g.17138147_17138148insTTAATGAGTCAATGTGGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138149_17138166dup , CM000678.2:g.17138149_17138166dup	GRCh38
NC_000016.9:g.17232006_17232023dup , CM000678.1:g.17232006_17232023dup	GRCh37
NC_000016.8:g.17139507_17139524dup	NCBI36
NG_015843.1:g.337717_337734dup
NG_015843.2:g.337717_337734dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+190_1764+207dup MANE Select	ENSP00000261381.6:n.1764+190_1764+207dup
ENST00000261381.6:c.1764+190_1764+207dup	ENSP00000261381.6:n.1764+190_1764+207dup
NM_022166.3:c.1764+190_1764+207dup	NP_071449.1:n.1764+190_1764+207dup
XM_011522574.1:c.1764+190_1764+207dup	XP_011520876.1:n.1764+190_1764+207dup
XR_933140.1:n.336-93_336-76dup
XR_933141.1:n.175-93_175-76dup
XR_933143.1:n.237-93_237-76dup
NR_135179.1:n.147-93_147-76dup
XM_017023539.2:c.1764+190_1764+207dup	XP_016879028.1:n.1764+190_1764+207dup
XM_017023540.2:c.1764+190_1764+207dup	XP_016879029.1:n.1764+190_1764+207dup
NM_022166.4:c.1764+190_1764+207dup MANE Select	NP_071449.1:n.1764+190_1764+207dup