Canonical Allele Identifier: CA2210542398
Gene: XYLT1 HGNC NCBI

Linked Data

dbSNP Id: rs2030858363
gnomAD v4: 16-17138617-G-GAGTTCATGTA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138620_17138629dup , CM000678.2:g.17138620_17138629dup GRCh38
NC_000016.9:g.17232477_17232486dup , CM000678.1:g.17232477_17232486dup GRCh37
NC_000016.8:g.17139978_17139987dup NCBI36
NG_015843.1:g.337255_337264dup
NG_015843.2:g.337255_337264dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1588-96_1588-87dup MANE Select ENSP00000261381.6:n.1588-96_1588-87dup
ENST00000261381.6:c.1588-96_1588-87dup ENSP00000261381.6:n.1588-96_1588-87dup
NM_022166.3:c.1588-96_1588-87dup NP_071449.1:n.1588-96_1588-87dup
XM_011522574.1:c.1588-96_1588-87dup XP_011520876.1:n.1588-96_1588-87dup
XR_933141.1:n.553_562dup
NR_135179.1:n.525_534dup
XM_017023539.2:c.1588-96_1588-87dup XP_016879028.1:n.1588-96_1588-87dup
XM_017023540.2:c.1588-96_1588-87dup XP_016879029.1:n.1588-96_1588-87dup
NM_022166.4:c.1588-96_1588-87dup MANE Select NP_071449.1:n.1588-96_1588-87dup
Search 100 bp 5'
Search 100 bp 3'