Canonical Allele Identifier: CA2631987557
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138505_17138564dup , CM000678.2:g.17138505_17138564dup GRCh38
NC_000016.9:g.17232362_17232421dup , CM000678.1:g.17232362_17232421dup GRCh37
NC_000016.8:g.17139863_17139922dup NCBI36
NG_015843.1:g.337320_337379dup
NG_015843.2:g.337320_337379dup

Transcript Alleles

HGVS Amino-acid change
ENST00000261381.7:c.1588-31_1616dup
ENST00000261381.6:c.1588-31_1616dup
NM_022166.3:c.1588-31_1616dup
XM_011522574.1:c.1588-31_1616dup
XR_933141.1:n.438_497dup
NR_135179.1:n.410_469dup
XM_017023539.2:c.1588-31_1616dup
XM_017023540.2:c.1588-31_1616dup
NM_022166.4:c.1588-31_1616dup