Canonical Allele Identifier: CA2631987563
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138545_17138571dup , CM000678.2:g.17138545_17138571dup GRCh38
NC_000016.9:g.17232402_17232428dup , CM000678.1:g.17232402_17232428dup GRCh37
NC_000016.8:g.17139903_17139929dup NCBI36
NG_015843.1:g.337313_337339dup
NG_015843.2:g.337313_337339dup

Transcript Alleles

HGVS Amino-acid change
ENST00000261381.7:c.1588-38_1588-12dup MANE Select ENSP00000261381.6:n.1588-38_1588-12dup
ENST00000261381.6:c.1588-38_1588-12dup ENSP00000261381.6:n.1588-38_1588-12dup
NM_022166.3:c.1588-38_1588-12dup NP_071449.1:n.1588-38_1588-12dup
XM_011522574.1:c.1588-38_1588-12dup XP_011520876.1:n.1588-38_1588-12dup
XR_933141.1:n.478_504dup
NR_135179.1:n.450_476dup
XM_017023539.2:c.1588-38_1588-12dup XP_016879028.1:n.1588-38_1588-12dup
XM_017023540.2:c.1588-38_1588-12dup XP_016879029.1:n.1588-38_1588-12dup
NM_022166.4:c.1588-38_1588-12dup MANE Select NP_071449.1:n.1588-38_1588-12dup