Canonical Allele Identifier: CA2631987559
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138522_17138542dup , CM000678.2:g.17138522_17138542dup GRCh38
NC_000016.9:g.17232379_17232399dup , CM000678.1:g.17232379_17232399dup GRCh37
NC_000016.8:g.17139880_17139900dup NCBI36
NG_015843.1:g.337340_337360dup
NG_015843.2:g.337340_337360dup

Transcript Alleles

HGVS Amino-acid change
ENST00000261381.7:c.1588-11_1597dup
ENST00000261381.6:c.1588-11_1597dup
NM_022166.3:c.1588-11_1597dup
XM_011522574.1:c.1588-11_1597dup
XR_933141.1:n.455_475dup
NR_135179.1:n.427_447dup
XM_017023539.2:c.1588-11_1597dup
XM_017023540.2:c.1588-11_1597dup
NM_022166.4:c.1588-11_1597dup