Canonical Allele Identifier: CA151428
Gene: XYLT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 127238
dbSNP Id: rs201818754

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138534G>A , CM000678.2:g.17138534G>A GRCh38
NC_000016.9:g.17232391G>A , CM000678.1:g.17232391G>A GRCh37
NC_000016.8:g.17139892G>A NCBI36
NG_015843.1:g.337348C>T
NG_015843.2:g.337348C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261381.7:c.1588-3C>T MANE Select ENSP00000261381.6:n.1588-3C>T
ENST00000261381.6:c.1588-3C>T ENSP00000261381.6:n.1588-3C>T
NM_022166.3:c.1588-3C>T NP_071449.1:n.1588-3C>T
XM_011522574.1:c.1588-3C>T XP_011520876.1:n.1588-3C>T
XR_933141.1:n.467G>A
NR_135179.1:n.439G>A
XM_017023539.2:c.1588-3C>T XP_016879028.1:n.1588-3C>T
XM_017023540.2:c.1588-3C>T XP_016879029.1:n.1588-3C>T
NM_022166.4:c.1588-3C>T MANE Select NP_071449.1:n.1588-3C>T