Canonical Allele Identifier: CA2631987545
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138329_17138337del , CM000678.2:g.17138329_17138337del GRCh38
NC_000016.9:g.17232186_17232194del , CM000678.1:g.17232186_17232194del GRCh37
NC_000016.8:g.17139687_17139695del NCBI36
NG_015843.1:g.337545_337553del
NG_015843.2:g.337545_337553del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1764+18_1764+26del MANE Select ENSP00000261381.6:n.1764+18_1764+26del
ENST00000261381.6:c.1764+18_1764+26del ENSP00000261381.6:n.1764+18_1764+26del
NM_022166.3:c.1764+18_1764+26del NP_071449.1:n.1764+18_1764+26del
XM_011522574.1:c.1764+18_1764+26del XP_011520876.1:n.1764+18_1764+26del
XR_933140.1:n.423_431del
XR_933141.1:n.262_270del
XR_933143.1:n.324_332del
NR_135179.1:n.234_242del
XM_017023539.2:c.1764+18_1764+26del XP_016879028.1:n.1764+18_1764+26del
XM_017023540.2:c.1764+18_1764+26del XP_016879029.1:n.1764+18_1764+26del
NM_022166.4:c.1764+18_1764+26del MANE Select NP_071449.1:n.1764+18_1764+26del