Canonical Allele Identifier: CA2631987283

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17138160-T-TGTGGTTA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138162_17138168dup , CM000678.2:g.17138162_17138168dup	GRCh38
NC_000016.9:g.17232019_17232025dup , CM000678.1:g.17232019_17232025dup	GRCh37
NC_000016.8:g.17139520_17139526dup	NCBI36
NG_015843.1:g.337715_337721dup
NG_015843.2:g.337715_337721dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+188_1764+194dup MANE Select	ENSP00000261381.6:n.1764+188_1764+194dup
ENST00000261381.6:c.1764+188_1764+194dup	ENSP00000261381.6:n.1764+188_1764+194dup
NM_022166.3:c.1764+188_1764+194dup	NP_071449.1:n.1764+188_1764+194dup
XM_011522574.1:c.1764+188_1764+194dup	XP_011520876.1:n.1764+188_1764+194dup
XR_933140.1:n.336-80_336-74dup
XR_933141.1:n.175-80_175-74dup
XR_933143.1:n.237-80_237-74dup
NR_135179.1:n.147-80_147-74dup
XM_017023539.2:c.1764+188_1764+194dup	XP_016879028.1:n.1764+188_1764+194dup
XM_017023540.2:c.1764+188_1764+194dup	XP_016879029.1:n.1764+188_1764+194dup
NM_022166.4:c.1764+188_1764+194dup MANE Select	NP_071449.1:n.1764+188_1764+194dup