Canonical Allele Identifier: CA2631986853

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17134438-T-TCAGCTCTCCTCTCTGCATC

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17134440_17134458dup , CM000678.2:g.17134440_17134458dup	GRCh38
NC_000016.9:g.17228297_17228315dup , CM000678.1:g.17228297_17228315dup	GRCh37
NC_000016.8:g.17135798_17135816dup	NCBI36
NG_015843.1:g.341425_341443dup
NG_015843.2:g.341425_341443dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.2027+16_2027+34dup MANE Select	ENSP00000261381.6:n.2027+16_2027+34dup
ENST00000261381.6:c.2027+16_2027+34dup	ENSP00000261381.6:n.2027+16_2027+34dup
NM_022166.3:c.2027+16_2027+34dup	NP_071449.1:n.2027+16_2027+34dup
XM_011522574.1:c.2027+16_2027+34dup	XP_011520876.1:n.2027+16_2027+34dup
XM_017023539.2:c.2027+16_2027+34dup	XP_016879028.1:n.2027+16_2027+34dup
XM_017023540.2:c.2027+16_2027+34dup	XP_016879029.1:n.2027+16_2027+34dup
NM_022166.4:c.2027+16_2027+34dup MANE Select	NP_071449.1:n.2027+16_2027+34dup