Canonical Allele Identifier: CA2631987265

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17138153-G-GAGTC

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138155_17138158dup , CM000678.2:g.17138155_17138158dup	GRCh38
NC_000016.9:g.17232012_17232015dup , CM000678.1:g.17232012_17232015dup	GRCh37
NC_000016.8:g.17139513_17139516dup	NCBI36
NG_015843.1:g.337725_337728dup
NG_015843.2:g.337725_337728dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+198_1764+201dup MANE Select	ENSP00000261381.6:n.1764+198_1764+201dup
ENST00000261381.6:c.1764+198_1764+201dup	ENSP00000261381.6:n.1764+198_1764+201dup
NM_022166.3:c.1764+198_1764+201dup	NP_071449.1:n.1764+198_1764+201dup
XM_011522574.1:c.1764+198_1764+201dup	XP_011520876.1:n.1764+198_1764+201dup
XR_933140.1:n.336-87_336-84dup
XR_933141.1:n.175-87_175-84dup
XR_933143.1:n.237-87_237-84dup
NR_135179.1:n.147-87_147-84dup
XM_017023539.2:c.1764+198_1764+201dup	XP_016879028.1:n.1764+198_1764+201dup
XM_017023540.2:c.1764+198_1764+201dup	XP_016879029.1:n.1764+198_1764+201dup
NM_022166.4:c.1764+198_1764+201dup MANE Select	NP_071449.1:n.1764+198_1764+201dup