Canonical Allele Identifier: CA718616954

Gene: XYLT1

Linked Data

• dbSNP Id: rs1377679514
• gnomAD v4: 16-17138581-G-GATGAACTGGGGTGGGAA
• MyVariant Identifiers: chr16:g.17232438_17232439insATGAACTGGGGTGGGAA (hg19) ; chr16:g.17138581_17138582insATGAACTGGGGTGGGAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138585_17138601dup , CM000678.2:g.17138585_17138601dup	GRCh38
NC_000016.9:g.17232442_17232458dup , CM000678.1:g.17232442_17232458dup	GRCh37
NC_000016.8:g.17139943_17139959dup	NCBI36
NG_015843.1:g.337284_337300dup
NG_015843.2:g.337284_337300dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-67_1588-51dup MANE Select	ENSP00000261381.6:n.1588-67_1588-51dup
ENST00000261381.6:c.1588-67_1588-51dup	ENSP00000261381.6:n.1588-67_1588-51dup
NM_022166.3:c.1588-67_1588-51dup	NP_071449.1:n.1588-67_1588-51dup
XM_011522574.1:c.1588-67_1588-51dup	XP_011520876.1:n.1588-67_1588-51dup
XR_933141.1:n.518_534dup
NR_135179.1:n.490_506dup
XM_017023539.2:c.1588-67_1588-51dup	XP_016879028.1:n.1588-67_1588-51dup
XM_017023540.2:c.1588-67_1588-51dup	XP_016879029.1:n.1588-67_1588-51dup
NM_022166.4:c.1588-67_1588-51dup MANE Select	NP_071449.1:n.1588-67_1588-51dup