Canonical Allele Identifier: CA2695222868
Gene: XYLT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138524_17138541del , CM000678.2:g.17138524_17138541del GRCh38
NC_000016.9:g.17232381_17232398del , CM000678.1:g.17232381_17232398del GRCh37
NC_000016.8:g.17139882_17139899del NCBI36
NG_015843.1:g.337341_337358del
NG_015843.2:g.337341_337358del

Transcript Alleles

HGVS Amino-acid change
ENST00000261381.7:c.1588-10_1595del
ENST00000261381.6:c.1588-10_1595del
NM_022166.3:c.1588-10_1595del
XM_011522574.1:c.1588-10_1595del
XR_933141.1:n.457_474del
NR_135179.1:n.429_446del
XM_017023539.2:c.1588-10_1595del
XM_017023540.2:c.1588-10_1595del
NM_022166.4:c.1588-10_1595del