Canonical Allele Identifier: CA919667547
Gene: XYLT1 HGNC NCBI

Linked Data

dbSNP Id: rs1567291516
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138543_17138546dup , CM000678.2:g.17138543_17138546dup GRCh38
NC_000016.9:g.17232400_17232403dup , CM000678.1:g.17232400_17232403dup GRCh37
NC_000016.8:g.17139901_17139904dup NCBI36
NG_015843.1:g.337339_337342dup
NG_015843.2:g.337339_337342dup

Transcript Alleles

HGVS Amino-acid change
ENST00000261381.7:c.1588-12_1588-9dup MANE Select ENSP00000261381.6:n.1588-12_1588-9dup
ENST00000261381.6:c.1588-12_1588-9dup ENSP00000261381.6:n.1588-12_1588-9dup
NM_022166.3:c.1588-12_1588-9dup NP_071449.1:n.1588-12_1588-9dup
XM_011522574.1:c.1588-12_1588-9dup XP_011520876.1:n.1588-12_1588-9dup
XR_933141.1:n.476_479dup
NR_135179.1:n.448_451dup
XM_017023539.2:c.1588-12_1588-9dup XP_016879028.1:n.1588-12_1588-9dup
XM_017023540.2:c.1588-12_1588-9dup XP_016879029.1:n.1588-12_1588-9dup
NM_022166.4:c.1588-12_1588-9dup MANE Select NP_071449.1:n.1588-12_1588-9dup
Search 100 bp 5'
Search 100 bp 3'