Canonical Allele Identifier: CA2210542196
Gene: XYLT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138541A= , CM000678.2:g.17138541A= GRCh38
NC_000016.9:g.17232398A= , CM000678.1:g.17232398A= GRCh37
NC_000016.8:g.17139899A= NCBI36
NG_015843.1:g.337341T=
NG_015843.2:g.337341T=

Transcript Alleles

HGVS Amino-acid change
ENST00000261381.7:c.1588-10T= MANE Select ENSP00000261381.6:n.1588-10T=
ENST00000261381.6:c.1588-10T= ENSP00000261381.6:n.1588-10T=
NM_022166.3:c.1588-10T= NP_071449.1:n.1588-10T=
XM_011522574.1:c.1588-10T= XP_011520876.1:n.1588-10T=
XR_933141.1:n.474A=
NR_135179.1:n.446A=
XM_017023539.2:c.1588-10T= XP_016879028.1:n.1588-10T=
XM_017023540.2:c.1588-10T= XP_016879029.1:n.1588-10T=
NM_022166.4:c.1588-10T= MANE Select NP_071449.1:n.1588-10T=