Canonical Allele Identifier: CA494103841
Gene: XYLT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.17228478G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17134621G>A , CM000678.2:g.17134621G>A GRCh38
NC_000016.9:g.17228478G>A , CM000678.1:g.17228478G>A GRCh37
NC_000016.8:g.17135979G>A NCBI36
NG_015843.1:g.341261C>T
NG_015843.2:g.341261C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261381.7:c.1879C>T MANE Select ENSP00000261381.6:p.Leu627=
ENST00000261381.6:c.1879C>T ENSP00000261381.6:p.Leu627=
NM_022166.3:c.1879C>T NP_071449.1:p.Leu627=
XM_011522574.1:c.1879C>T XP_011520876.1:p.Leu627=
XR_933140.1:n.82+71G>A
XR_933141.1:n.75+71G>A
XR_933143.1:n.82+71G>A
NR_135179.1:n.47+71G>A
XM_017023539.2:c.1879C>T XP_016879028.1:p.Leu627=
XM_017023540.2:c.1879C>T XP_016879029.1:p.Leu627=
NM_022166.4:c.1879C>T MANE Select NP_071449.1:p.Leu627=