Canonical Allele Identifier: CA2631987544
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138330_17138363dup , CM000678.2:g.17138330_17138363dup GRCh38
NC_000016.9:g.17232187_17232220dup , CM000678.1:g.17232187_17232220dup GRCh37
NC_000016.8:g.17139688_17139721dup NCBI36
NG_015843.1:g.337520_337553dup
NG_015843.2:g.337520_337553dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1757_1764+26dup
ENST00000261381.6:c.1757_1764+26dup
NM_022166.3:c.1757_1764+26dup
XM_011522574.1:c.1757_1764+26dup
XR_933141.1:n.263_296dup
NR_135179.1:n.235_268dup
XM_017023539.2:c.1757_1764+26dup
XM_017023540.2:c.1757_1764+26dup
NM_022166.4:c.1757_1764+26dup