Canonical Allele Identifier: CA278644376

Gene: XYLT1

Linked Data

• dbSNP Id: rs774995120
• MyVariant Identifiers: chr16:g.17232181_17232193del (hg19) ; chr16:g.17138324_17138336del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138325_17138337del , CM000678.2:g.17138325_17138337del	GRCh38
NC_000016.9:g.17232182_17232194del , CM000678.1:g.17232182_17232194del	GRCh37
NC_000016.8:g.17139683_17139695del	NCBI36
NG_015843.1:g.337546_337558del
NG_015843.2:g.337546_337558del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+19_1764+31del MANE Select	ENSP00000261381.6:n.1764+19_1764+31del
ENST00000261381.6:c.1764+19_1764+31del	ENSP00000261381.6:n.1764+19_1764+31del
NM_022166.3:c.1764+19_1764+31del	NP_071449.1:n.1764+19_1764+31del
XM_011522574.1:c.1764+19_1764+31del	XP_011520876.1:n.1764+19_1764+31del
XR_933140.1:n.419_431del
XR_933141.1:n.258_270del
XR_933143.1:n.320_332del
NR_135179.1:n.230_242del
XM_017023539.2:c.1764+19_1764+31del	XP_016879028.1:n.1764+19_1764+31del
XM_017023540.2:c.1764+19_1764+31del	XP_016879029.1:n.1764+19_1764+31del
NM_022166.4:c.1764+19_1764+31del MANE Select	NP_071449.1:n.1764+19_1764+31del