Canonical Allele Identifier: CA278644911

Gene: XYLT1

Linked Data

• dbSNP Id: rs888101286
• gnomAD v2: 16-17232659-CTT-C
• gnomAD v3: 16-17138802-CTT-C
• gnomAD v4: 16-17138802-CTT-C
• MyVariant Identifiers: chr16:g.17232660_17232661del (hg19) ; chr16:g.17138803_17138804del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138803_17138804del , CM000678.2:g.17138803_17138804del	GRCh38
NC_000016.9:g.17232660_17232661del , CM000678.1:g.17232660_17232661del	GRCh37
NC_000016.8:g.17140161_17140162del	NCBI36
NG_015843.1:g.337078_337079del
NG_015843.2:g.337078_337079del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-273_1588-272del MANE Select	ENSP00000261381.6:n.1588-273_1588-272del
ENST00000261381.6:c.1588-273_1588-272del	ENSP00000261381.6:n.1588-273_1588-272del
NM_022166.3:c.1588-273_1588-272del	NP_071449.1:n.1588-273_1588-272del
XM_011522574.1:c.1588-273_1588-272del	XP_011520876.1:n.1588-273_1588-272del
XM_017023539.2:c.1588-273_1588-272del	XP_016879028.1:n.1588-273_1588-272del
XM_017023540.2:c.1588-273_1588-272del	XP_016879029.1:n.1588-273_1588-272del
NM_022166.4:c.1588-273_1588-272del MANE Select	NP_071449.1:n.1588-273_1588-272del