Canonical Allele Identifier: CA2210541999
Gene: XYLT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138445C= , CM000678.2:g.17138445C= GRCh38
NC_000016.9:g.17232302C= , CM000678.1:g.17232302C= GRCh37
NC_000016.8:g.17139803C= NCBI36
NG_015843.1:g.337437G=
NG_015843.2:g.337437G=

Transcript Alleles

HGVS Amino-acid change
ENST00000261381.7:c.1674G= MANE Select ENSP00000261381.6:p.Lys558=
ENST00000261381.6:c.1674G= ENSP00000261381.6:p.Lys558=
NM_022166.3:c.1674G= NP_071449.1:p.Lys558=
XM_011522574.1:c.1674G= XP_011520876.1:p.Lys558=
XR_933141.1:n.378C=
NR_135179.1:n.350C=
XM_017023539.2:c.1674G= XP_016879028.1:p.Lys558=
XM_017023540.2:c.1674G= XP_016879029.1:p.Lys558=
NM_022166.4:c.1674G= MANE Select NP_071449.1:p.Lys558=