Canonical Allele Identifier: CA2631987548
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138345_17138377dup , CM000678.2:g.17138345_17138377dup GRCh38
NC_000016.9:g.17232202_17232234dup , CM000678.1:g.17232202_17232234dup GRCh37
NC_000016.8:g.17139703_17139735dup NCBI36
NG_015843.1:g.337506_337538dup
NG_015843.2:g.337506_337538dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1743_1764+11dup
ENST00000261381.6:c.1743_1764+11dup
NM_022166.3:c.1743_1764+11dup
XM_011522574.1:c.1743_1764+11dup
XR_933141.1:n.278_310dup
NR_135179.1:n.250_282dup
XM_017023539.2:c.1743_1764+11dup
XM_017023540.2:c.1743_1764+11dup
NM_022166.4:c.1743_1764+11dup