Canonical Allele Identifier: CA2592164509
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17134716_17134747dup , CM000678.2:g.17134716_17134747dup GRCh38
NC_000016.9:g.17228573_17228604dup , CM000678.1:g.17228573_17228604dup GRCh37
NC_000016.8:g.17136074_17136105dup NCBI36
NG_015843.1:g.341136_341167dup
NG_015843.2:g.341136_341167dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1765-11_1785dup
ENST00000261381.6:c.1765-11_1785dup
NM_022166.3:c.1765-11_1785dup
XM_011522574.1:c.1765-11_1785dup
XR_933140.1:n.82+166_82+197dup
XR_933141.1:n.75+166_75+197dup
XR_933143.1:n.82+166_82+197dup
NR_135179.1:n.47+166_47+197dup
XM_017023539.2:c.1765-11_1785dup
XM_017023540.2:c.1765-11_1785dup
NM_022166.4:c.1765-11_1785dup