Canonical Allele Identifier: CA2210542003
Gene: XYLT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138447T= , CM000678.2:g.17138447T= GRCh38
NC_000016.9:g.17232304T= , CM000678.1:g.17232304T= GRCh37
NC_000016.8:g.17139805T= NCBI36
NG_015843.1:g.337435A=
NG_015843.2:g.337435A=

Transcript Alleles

HGVS Amino-acid change
ENST00000261381.7:c.1672A= MANE Select ENSP00000261381.6:p.Lys558=
ENST00000261381.6:c.1672A= ENSP00000261381.6:p.Lys558=
NM_022166.3:c.1672A= NP_071449.1:p.Lys558=
XM_011522574.1:c.1672A= XP_011520876.1:p.Lys558=
XR_933141.1:n.380T=
NR_135179.1:n.352T=
XM_017023539.2:c.1672A= XP_016879028.1:p.Lys558=
XM_017023540.2:c.1672A= XP_016879029.1:p.Lys558=
NM_022166.4:c.1672A= MANE Select NP_071449.1:p.Lys558=