Canonical Allele Identifier: CA2631986870

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17134745-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17134748del , CM000678.2:g.17134748del	GRCh38
NC_000016.9:g.17228605del , CM000678.1:g.17228605del	GRCh37
NC_000016.8:g.17136106del	NCBI36
NG_015843.1:g.341136del
NG_015843.2:g.341136del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1765-11del MANE Select	ENSP00000261381.6:n.1765-11del
ENST00000261381.6:c.1765-11del	ENSP00000261381.6:n.1765-11del
NM_022166.3:c.1765-11del	NP_071449.1:n.1765-11del
XM_011522574.1:c.1765-11del	XP_011520876.1:n.1765-11del
XR_933140.1:n.82+198del
XR_933141.1:n.75+198del
XR_933143.1:n.82+198del
NR_135179.1:n.47+198del
XM_017023539.2:c.1765-11del	XP_016879028.1:n.1765-11del
XM_017023540.2:c.1765-11del	XP_016879029.1:n.1765-11del
NM_022166.4:c.1765-11del MANE Select	NP_071449.1:n.1765-11del