Canonical Allele Identifier: CA2631986864
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17134599_17134609dup , CM000678.2:g.17134599_17134609dup GRCh38
NC_000016.9:g.17228456_17228466dup , CM000678.1:g.17228456_17228466dup GRCh37
NC_000016.8:g.17135957_17135967dup NCBI36
NG_015843.1:g.341273_341283dup
NG_015843.2:g.341273_341283dup

Transcript Alleles

HGVS Amino-acid change
ENST00000261381.7:c.1891_1901dup MANE Select ENSP00000261381.6:p.Tyr635GlyfsTer14
ENST00000261381.6:c.1891_1901dup ENSP00000261381.6:p.Tyr635GlyfsTer14
NM_022166.3:c.1891_1901dup NP_071449.1:p.Tyr635GlyfsTer14
XM_011522574.1:c.1891_1901dup XP_011520876.1:p.Tyr635GlyfsTer14
XR_933140.1:n.82+49_82+59dup
XR_933141.1:n.75+49_75+59dup
XR_933143.1:n.82+49_82+59dup
NR_135179.1:n.47+49_47+59dup
XM_017023539.2:c.1891_1901dup XP_016879028.1:p.Tyr635GlyfsTer14
XM_017023540.2:c.1891_1901dup XP_016879029.1:p.Tyr635GlyfsTer14
NM_022166.4:c.1891_1901dup MANE Select NP_071449.1:p.Tyr635GlyfsTer14