Canonical Allele Identifier: CA2210541461

Gene: XYLT1

Linked Data

• dbSNP Id: rs2030820418
• gnomAD v3: 16-17138136-G-GTTGTT
• gnomAD v4: 16-17138136-G-GTTGTT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138139_17138143dup , CM000678.2:g.17138139_17138143dup	GRCh38
NC_000016.9:g.17231996_17232000dup , CM000678.1:g.17231996_17232000dup	GRCh37
NC_000016.8:g.17139497_17139501dup	NCBI36
NG_015843.1:g.337741_337745dup
NG_015843.2:g.337741_337745dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+214_1764+218dup MANE Select	ENSP00000261381.6:n.1764+214_1764+218dup
ENST00000261381.6:c.1764+214_1764+218dup	ENSP00000261381.6:n.1764+214_1764+218dup
NM_022166.3:c.1764+214_1764+218dup	NP_071449.1:n.1764+214_1764+218dup
XM_011522574.1:c.1764+214_1764+218dup	XP_011520876.1:n.1764+214_1764+218dup
XR_933140.1:n.336-103_336-99dup
XR_933141.1:n.175-103_175-99dup
XR_933143.1:n.237-103_237-99dup
NR_135179.1:n.147-103_147-99dup
XM_017023539.2:c.1764+214_1764+218dup	XP_016879028.1:n.1764+214_1764+218dup
XM_017023540.2:c.1764+214_1764+218dup	XP_016879029.1:n.1764+214_1764+218dup
NM_022166.4:c.1764+214_1764+218dup MANE Select	NP_071449.1:n.1764+214_1764+218dup