Canonical Allele Identifier: CA975205912
Gene: XYLT1 HGNC NCBI

Linked Data

dbSNP Id: rs2030855629

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138577_17138588dup , CM000678.2:g.17138577_17138588dup GRCh38
NC_000016.9:g.17232434_17232445dup , CM000678.1:g.17232434_17232445dup GRCh37
NC_000016.8:g.17139935_17139946dup NCBI36
NG_015843.1:g.337294_337305dup
NG_015843.2:g.337294_337305dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1588-57_1588-46dup MANE Select ENSP00000261381.6:n.1588-57_1588-46dup
ENST00000261381.6:c.1588-57_1588-46dup ENSP00000261381.6:n.1588-57_1588-46dup
NM_022166.3:c.1588-57_1588-46dup NP_071449.1:n.1588-57_1588-46dup
XM_011522574.1:c.1588-57_1588-46dup XP_011520876.1:n.1588-57_1588-46dup
XR_933141.1:n.510_521dup
NR_135179.1:n.482_493dup
XM_017023539.2:c.1588-57_1588-46dup XP_016879028.1:n.1588-57_1588-46dup
XM_017023540.2:c.1588-57_1588-46dup XP_016879029.1:n.1588-57_1588-46dup
NM_022166.4:c.1588-57_1588-46dup MANE Select NP_071449.1:n.1588-57_1588-46dup