Canonical Allele Identifier: CA975205653

Gene: XYLT1

Linked Data

• dbSNP Id: rs2030827461
• gnomAD v3: 16-17138224-ATTAT-A
• gnomAD v4: 16-17138224-ATTAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138226_17138229del , CM000678.2:g.17138226_17138229del	GRCh38
NC_000016.9:g.17232083_17232086del , CM000678.1:g.17232083_17232086del	GRCh37
NC_000016.8:g.17139584_17139587del	NCBI36
NG_015843.1:g.337654_337657del
NG_015843.2:g.337654_337657del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+127_1764+130del MANE Select	ENSP00000261381.6:n.1764+127_1764+130del
ENST00000261381.6:c.1764+127_1764+130del	ENSP00000261381.6:n.1764+127_1764+130del
NM_022166.3:c.1764+127_1764+130del	NP_071449.1:n.1764+127_1764+130del
XM_011522574.1:c.1764+127_1764+130del	XP_011520876.1:n.1764+127_1764+130del
XR_933140.1:n.336-16_336-13del
XR_933141.1:n.175-16_175-13del
XR_933143.1:n.237-16_237-13del
NR_135179.1:n.147-16_147-13del
XM_017023539.2:c.1764+127_1764+130del	XP_016879028.1:n.1764+127_1764+130del
XM_017023540.2:c.1764+127_1764+130del	XP_016879029.1:n.1764+127_1764+130del
NM_022166.4:c.1764+127_1764+130del MANE Select	NP_071449.1:n.1764+127_1764+130del