Canonical Allele Identifier: CA2570287624

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17134769-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17134770dup , CM000678.2:g.17134770dup	GRCh38
NC_000016.9:g.17228627dup , CM000678.1:g.17228627dup	GRCh37
NC_000016.8:g.17136128dup	NCBI36
NG_015843.1:g.341112dup
NG_015843.2:g.341112dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1765-35dup MANE Select	ENSP00000261381.6:n.1765-35dup
ENST00000261381.6:c.1765-35dup	ENSP00000261381.6:n.1765-35dup
NM_022166.3:c.1765-35dup	NP_071449.1:n.1765-35dup
XM_011522574.1:c.1765-35dup	XP_011520876.1:n.1765-35dup
XR_933140.1:n.82+220dup
XR_933141.1:n.75+220dup
XR_933143.1:n.82+220dup
NR_135179.1:n.47+220dup
XM_017023539.2:c.1765-35dup	XP_016879028.1:n.1765-35dup
XM_017023540.2:c.1765-35dup	XP_016879029.1:n.1765-35dup
NM_022166.4:c.1765-35dup MANE Select	NP_071449.1:n.1765-35dup