Canonical Allele Identifier: CA2631987538
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138319_17138362dup , CM000678.2:g.17138319_17138362dup GRCh38
NC_000016.9:g.17232176_17232219dup , CM000678.1:g.17232176_17232219dup GRCh37
NC_000016.8:g.17139677_17139720dup NCBI36
NG_015843.1:g.337520_337563dup
NG_015843.2:g.337520_337563dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1757_1764+36dup
ENST00000261381.6:c.1757_1764+36dup
NM_022166.3:c.1757_1764+36dup
XM_011522574.1:c.1757_1764+36dup
XR_933141.1:n.252_295dup
NR_135179.1:n.224_267dup
XM_017023539.2:c.1757_1764+36dup
XM_017023540.2:c.1757_1764+36dup
NM_022166.4:c.1757_1764+36dup