Canonical Allele Identifier: CA2210538774
Gene: XYLT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17134617C= , CM000678.2:g.17134617C= GRCh38
NC_000016.9:g.17228474C= , CM000678.1:g.17228474C= GRCh37
NC_000016.8:g.17135975C= NCBI36
NG_015843.1:g.341265G=
NG_015843.2:g.341265G=

Transcript Alleles

HGVS Amino-acid change
ENST00000261381.7:c.1883G= MANE Select ENSP00000261381.6:p.Arg628=
ENST00000261381.6:c.1883G= ENSP00000261381.6:p.Arg628=
NM_022166.3:c.1883G= NP_071449.1:p.Arg628=
XM_011522574.1:c.1883G= XP_011520876.1:p.Arg628=
XR_933140.1:n.82+67C=
XR_933141.1:n.75+67C=
XR_933143.1:n.82+67C=
NR_135179.1:n.47+67C=
XM_017023539.2:c.1883G= XP_016879028.1:p.Arg628=
XM_017023540.2:c.1883G= XP_016879029.1:p.Arg628=
NM_022166.4:c.1883G= MANE Select NP_071449.1:p.Arg628=