Canonical Allele Identifier: CA2631987572
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138579_17138585del , CM000678.2:g.17138579_17138585del GRCh38
NC_000016.9:g.17232436_17232442del , CM000678.1:g.17232436_17232442del GRCh37
NC_000016.8:g.17139937_17139943del NCBI36
NG_015843.1:g.337298_337304del
NG_015843.2:g.337298_337304del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1588-53_1588-47del MANE Select ENSP00000261381.6:n.1588-53_1588-47del
ENST00000261381.6:c.1588-53_1588-47del ENSP00000261381.6:n.1588-53_1588-47del
NM_022166.3:c.1588-53_1588-47del NP_071449.1:n.1588-53_1588-47del
XM_011522574.1:c.1588-53_1588-47del XP_011520876.1:n.1588-53_1588-47del
XR_933141.1:n.512_518del
NR_135179.1:n.484_490del
XM_017023539.2:c.1588-53_1588-47del XP_016879028.1:n.1588-53_1588-47del
XM_017023540.2:c.1588-53_1588-47del XP_016879029.1:n.1588-53_1588-47del
NM_022166.4:c.1588-53_1588-47del MANE Select NP_071449.1:n.1588-53_1588-47del