Canonical Allele Identifier: CA394875108
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138360A>C , CM000678.2:g.17138360A>C GRCh38
NC_000016.9:g.17232217A>C , CM000678.1:g.17232217A>C GRCh37
NC_000016.8:g.17139718A>C NCBI36
NG_015843.1:g.337522T>G
NG_015843.2:g.337522T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1759T>G MANE Select ENSP00000261381.6:p.Phe587Val
ENST00000261381.6:c.1759T>G ENSP00000261381.6:p.Phe587Val
NM_022166.3:c.1759T>G NP_071449.1:p.Phe587Val
XM_011522574.1:c.1759T>G XP_011520876.1:p.Phe587Val
XR_933141.1:n.293A>C
NR_135179.1:n.265A>C
XM_017023539.2:c.1759T>G XP_016879028.1:p.Phe587Val
XM_017023540.2:c.1759T>G XP_016879029.1:p.Phe587Val
NM_022166.4:c.1759T>G MANE Select NP_071449.1:p.Phe587Val