Canonical Allele Identifier: CA395219565
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17134600C>A , CM000678.2:g.17134600C>A GRCh38
NC_000016.9:g.17228457C>A , CM000678.1:g.17228457C>A GRCh37
NC_000016.8:g.17135958C>A NCBI36
NG_015843.1:g.341282G>T
NG_015843.2:g.341282G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1900G>T MANE Select ENSP00000261381.6:p.Val634Phe
ENST00000261381.6:c.1900G>T ENSP00000261381.6:p.Val634Phe
NM_022166.3:c.1900G>T NP_071449.1:p.Val634Phe
XM_011522574.1:c.1900G>T XP_011520876.1:p.Val634Phe
XR_933140.1:n.82+50C>A
XR_933141.1:n.75+50C>A
XR_933143.1:n.82+50C>A
NR_135179.1:n.47+50C>A
XM_017023539.2:c.1900G>T XP_016879028.1:p.Val634Phe
XM_017023540.2:c.1900G>T XP_016879029.1:p.Val634Phe
NM_022166.4:c.1900G>T MANE Select NP_071449.1:p.Val634Phe