Canonical Allele Identifier: CA2631987553
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138445_17138471del , CM000678.2:g.17138445_17138471del GRCh38
NC_000016.9:g.17232302_17232328del , CM000678.1:g.17232302_17232328del GRCh37
NC_000016.8:g.17139803_17139829del NCBI36
NG_015843.1:g.337414_337440del
NG_015843.2:g.337414_337440del

Transcript Alleles

HGVS Amino-acid change
ENST00000261381.7:c.1651_1677del MANE Select ENSP00000261381.6:p.Arg551_Leu559del
ENST00000261381.6:c.1651_1677del ENSP00000261381.6:p.Arg551_Leu559del
NM_022166.3:c.1651_1677del NP_071449.1:p.Arg551_Leu559del
XM_011522574.1:c.1651_1677del XP_011520876.1:p.Arg551_Leu559del
XR_933141.1:n.378_404del
NR_135179.1:n.350_376del
XM_017023539.2:c.1651_1677del XP_016879028.1:p.Arg551_Leu559del
XM_017023540.2:c.1651_1677del XP_016879029.1:p.Arg551_Leu559del
NM_022166.4:c.1651_1677del MANE Select NP_071449.1:p.Arg551_Leu559del