Canonical Allele Identifier: CA2631987562
Gene: XYLT1 HGNC NCBI

Linked Data

gnomAD v4: 16-17138537-G-GGGGAGAGAGGGACCCAGCCTGAGACCTCTCCCAGCCTCCCACAGATGAACT
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138541_17138591dup , CM000678.2:g.17138541_17138591dup GRCh38
NC_000016.9:g.17232398_17232448dup , CM000678.1:g.17232398_17232448dup GRCh37
NC_000016.8:g.17139899_17139949dup NCBI36
NG_015843.1:g.337294_337344dup
NG_015843.2:g.337294_337344dup

Transcript Alleles

HGVS Amino-acid change
ENST00000261381.7:c.1588-57_1588-7dup MANE Select ENSP00000261381.6:n.1588-57_1588-7dup
ENST00000261381.6:c.1588-57_1588-7dup ENSP00000261381.6:n.1588-57_1588-7dup
NM_022166.3:c.1588-57_1588-7dup NP_071449.1:n.1588-57_1588-7dup
XM_011522574.1:c.1588-57_1588-7dup XP_011520876.1:n.1588-57_1588-7dup
XR_933141.1:n.474_524dup
NR_135179.1:n.446_496dup
XM_017023539.2:c.1588-57_1588-7dup XP_016879028.1:n.1588-57_1588-7dup
XM_017023540.2:c.1588-57_1588-7dup XP_016879029.1:n.1588-57_1588-7dup
NM_022166.4:c.1588-57_1588-7dup MANE Select NP_071449.1:n.1588-57_1588-7dup
Search 100 bp 5'
Search 100 bp 3'