Canonical Allele Identifier: CA2210542925
Gene: XYLT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138917_17138922delinsGTGTGC , CM000678.2:g.17138917_17138922delinsGTGTGC GRCh38
NC_000016.9:g.17232774_17232779delinsGTGTGC , CM000678.1:g.17232774_17232779delinsGTGTGC GRCh37
NC_000016.8:g.17140275_17140280delinsGTGTGC NCBI36
NG_015843.1:g.336960_336965delinsGCACAC
NG_015843.2:g.336960_336965delinsGCACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1588-391_1588-386delinsGCACAC MANE Select ENSP00000261381.6:n.1588-391_1588-386delinsGCACAC
ENST00000261381.6:c.1588-391_1588-386delinsGCACAC ENSP00000261381.6:n.1588-391_1588-386delinsGCACAC
NM_022166.3:c.1588-391_1588-386delinsGCACAC NP_071449.1:n.1588-391_1588-386delinsGCACAC
XM_011522574.1:c.1588-391_1588-386delinsGCACAC XP_011520876.1:n.1588-391_1588-386delinsGCACAC
XM_017023539.2:c.1588-391_1588-386delinsGCACAC XP_016879028.1:n.1588-391_1588-386delinsGCACAC
XM_017023540.2:c.1588-391_1588-386delinsGCACAC XP_016879029.1:n.1588-391_1588-386delinsGCACAC
NM_022166.4:c.1588-391_1588-386delinsGCACAC MANE Select NP_071449.1:n.1588-391_1588-386delinsGCACAC