Canonical Allele Identifier: CA2631987555

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17138467-C-CGCAGGTTG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138468_17138475dup , CM000678.2:g.17138468_17138475dup	GRCh38
NC_000016.9:g.17232325_17232332dup , CM000678.1:g.17232325_17232332dup	GRCh37
NC_000016.8:g.17139826_17139833dup	NCBI36
NG_015843.1:g.337407_337414dup
NG_015843.2:g.337407_337414dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1644_1651dup MANE Select	ENSP00000261381.6:p.Arg551ProfsTer?
ENST00000261381.6:c.1644_1651dup	ENSP00000261381.6:p.Arg551ProfsTer?
NM_022166.3:c.1644_1651dup	NP_071449.1:p.Arg551ProfsTer?
XM_011522574.1:c.1644_1651dup	XP_011520876.1:p.Arg551ProfsTer?
XR_933141.1:n.401_408dup
NR_135179.1:n.373_380dup
XM_017023539.2:c.1644_1651dup	XP_016879028.1:p.Arg551ProfsTer?
XM_017023540.2:c.1644_1651dup	XP_016879029.1:p.Arg551ProfsTer?
NM_022166.4:c.1644_1651dup MANE Select	NP_071449.1:p.Arg551ProfsTer?