Canonical Allele Identifier: CA394875114
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138363G>T , CM000678.2:g.17138363G>T GRCh38
NC_000016.9:g.17232220G>T , CM000678.1:g.17232220G>T GRCh37
NC_000016.8:g.17139721G>T NCBI36
NG_015843.1:g.337519C>A
NG_015843.2:g.337519C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1756C>A MANE Select ENSP00000261381.6:p.Arg586Ser
ENST00000261381.6:c.1756C>A ENSP00000261381.6:p.Arg586Ser
NM_022166.3:c.1756C>A NP_071449.1:p.Arg586Ser
XM_011522574.1:c.1756C>A XP_011520876.1:p.Arg586Ser
XR_933141.1:n.296G>T
NR_135179.1:n.268G>T
XM_017023539.2:c.1756C>A XP_016879028.1:p.Arg586Ser
XM_017023540.2:c.1756C>A XP_016879029.1:p.Arg586Ser
NM_022166.4:c.1756C>A MANE Select NP_071449.1:p.Arg586Ser