Canonical Allele Identifier: CA2210538771
Gene: XYLT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17134609A= , CM000678.2:g.17134609A= GRCh38
NC_000016.9:g.17228466A= , CM000678.1:g.17228466A= GRCh37
NC_000016.8:g.17135967A= NCBI36
NG_015843.1:g.341273T=
NG_015843.2:g.341273T=

Transcript Alleles

HGVS Amino-acid change
ENST00000261381.7:c.1891T= MANE Select ENSP00000261381.6:p.Trp631=
ENST00000261381.6:c.1891T= ENSP00000261381.6:p.Trp631=
NM_022166.3:c.1891T= NP_071449.1:p.Trp631=
XM_011522574.1:c.1891T= XP_011520876.1:p.Trp631=
XR_933140.1:n.82+59A=
XR_933141.1:n.75+59A=
XR_933143.1:n.82+59A=
NR_135179.1:n.47+59A=
XM_017023539.2:c.1891T= XP_016879028.1:p.Trp631=
XM_017023540.2:c.1891T= XP_016879029.1:p.Trp631=
NM_022166.4:c.1891T= MANE Select NP_071449.1:p.Trp631=