Canonical Allele Identifier: CA2631987590

Gene: XYLT1

Linked Data

• dbSNP Id: rs2141516096
• gnomAD v4: 16-17138632-C-CTGGT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138635_17138638dup , CM000678.2:g.17138635_17138638dup	GRCh38
NC_000016.9:g.17232492_17232495dup , CM000678.1:g.17232492_17232495dup	GRCh37
NC_000016.8:g.17139993_17139996dup	NCBI36
NG_015843.1:g.337246_337249dup
NG_015843.2:g.337246_337249dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-105_1588-102dup MANE Select	ENSP00000261381.6:n.1588-105_1588-102dup
ENST00000261381.6:c.1588-105_1588-102dup	ENSP00000261381.6:n.1588-105_1588-102dup
NM_022166.3:c.1588-105_1588-102dup	NP_071449.1:n.1588-105_1588-102dup
XM_011522574.1:c.1588-105_1588-102dup	XP_011520876.1:n.1588-105_1588-102dup
XR_933141.1:n.568_571dup
NR_135179.1:n.540_543dup
XM_017023539.2:c.1588-105_1588-102dup	XP_016879028.1:n.1588-105_1588-102dup
XM_017023540.2:c.1588-105_1588-102dup	XP_016879029.1:n.1588-105_1588-102dup
NM_022166.4:c.1588-105_1588-102dup MANE Select	NP_071449.1:n.1588-105_1588-102dup