Canonical Allele Identifier: CA2210542274

Gene: XYLT1

Linked Data

• dbSNP Id: rs2030855070

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138570_17138591dup , CM000678.2:g.17138570_17138591dup	GRCh38
NC_000016.9:g.17232427_17232448dup , CM000678.1:g.17232427_17232448dup	GRCh37
NC_000016.8:g.17139928_17139949dup	NCBI36
NG_015843.1:g.337291_337312dup
NG_015843.2:g.337291_337312dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-60_1588-39dup MANE Select	ENSP00000261381.6:n.1588-60_1588-39dup
ENST00000261381.6:c.1588-60_1588-39dup	ENSP00000261381.6:n.1588-60_1588-39dup
NM_022166.3:c.1588-60_1588-39dup	NP_071449.1:n.1588-60_1588-39dup
XM_011522574.1:c.1588-60_1588-39dup	XP_011520876.1:n.1588-60_1588-39dup
XR_933141.1:n.503_524dup
NR_135179.1:n.475_496dup
XM_017023539.2:c.1588-60_1588-39dup	XP_016879028.1:n.1588-60_1588-39dup
XM_017023540.2:c.1588-60_1588-39dup	XP_016879029.1:n.1588-60_1588-39dup
NM_022166.4:c.1588-60_1588-39dup MANE Select	NP_071449.1:n.1588-60_1588-39dup