Canonical Allele Identifier: CA2631987621

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17138720-TCTTTATAAATTACCAAGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138723_17138740del , CM000678.2:g.17138723_17138740del	GRCh38
NC_000016.9:g.17232580_17232597del , CM000678.1:g.17232580_17232597del	GRCh37
NC_000016.8:g.17140081_17140098del	NCBI36
NG_015843.1:g.337144_337161del
NG_015843.2:g.337144_337161del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-207_1588-190del MANE Select	ENSP00000261381.6:n.1588-207_1588-190del
ENST00000261381.6:c.1588-207_1588-190del	ENSP00000261381.6:n.1588-207_1588-190del
NM_022166.3:c.1588-207_1588-190del	NP_071449.1:n.1588-207_1588-190del
XM_011522574.1:c.1588-207_1588-190del	XP_011520876.1:n.1588-207_1588-190del
XM_017023539.2:c.1588-207_1588-190del	XP_016879028.1:n.1588-207_1588-190del
XM_017023540.2:c.1588-207_1588-190del	XP_016879029.1:n.1588-207_1588-190del
NM_022166.4:c.1588-207_1588-190del MANE Select	NP_071449.1:n.1588-207_1588-190del