Canonical Allele Identifier: CA2631987561
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138528_17138567dup , CM000678.2:g.17138528_17138567dup GRCh38
NC_000016.9:g.17232385_17232424dup , CM000678.1:g.17232385_17232424dup GRCh37
NC_000016.8:g.17139886_17139925dup NCBI36
NG_015843.1:g.337315_337354dup
NG_015843.2:g.337315_337354dup

Transcript Alleles

HGVS Amino-acid change
ENST00000261381.7:c.1588-36_1591dup
ENST00000261381.6:c.1588-36_1591dup
NM_022166.3:c.1588-36_1591dup
XM_011522574.1:c.1588-36_1591dup
XR_933141.1:n.461_500dup
NR_135179.1:n.433_472dup
XM_017023539.2:c.1588-36_1591dup
XM_017023540.2:c.1588-36_1591dup
NM_022166.4:c.1588-36_1591dup