Canonical Allele Identifier: CA278644515
Gene: XYLT1 HGNC NCBI

Linked Data

dbSNP Id: rs866284538

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000261381.7:c.1674G>T MANE Select ENSP00000261381.6:p.Lys558Asn
ENST00000261381.6:c.1674G>T ENSP00000261381.6:p.Lys558Asn
NM_022166.3:c.1674G>T NP_071449.1:p.Lys558Asn
XM_011522574.1:c.1674G>T XP_011520876.1:p.Lys558Asn
XR_933141.1:n.378C>A
NR_135179.1:n.350C>A
XM_017023539.2:c.1674G>T XP_016879028.1:p.Lys558Asn
XM_017023540.2:c.1674G>T XP_016879029.1:p.Lys558Asn
NM_022166.4:c.1674G>T MANE Select NP_071449.1:p.Lys558Asn