Canonical Allele Identifier: CA975206079
Gene: XYLT1 HGNC NCBI

Linked Data

dbSNP Id: rs2030870234

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138827_17138831dup , CM000678.2:g.17138827_17138831dup GRCh38
NC_000016.9:g.17232684_17232688dup , CM000678.1:g.17232684_17232688dup GRCh37
NC_000016.8:g.17140185_17140189dup NCBI36
NG_015843.1:g.337053_337057dup
NG_015843.2:g.337053_337057dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1588-298_1588-294dup MANE Select ENSP00000261381.6:n.1588-298_1588-294dup
ENST00000261381.6:c.1588-298_1588-294dup ENSP00000261381.6:n.1588-298_1588-294dup
NM_022166.3:c.1588-298_1588-294dup NP_071449.1:n.1588-298_1588-294dup
XM_011522574.1:c.1588-298_1588-294dup XP_011520876.1:n.1588-298_1588-294dup
XM_017023539.2:c.1588-298_1588-294dup XP_016879028.1:n.1588-298_1588-294dup
XM_017023540.2:c.1588-298_1588-294dup XP_016879029.1:n.1588-298_1588-294dup
NM_022166.4:c.1588-298_1588-294dup MANE Select NP_071449.1:n.1588-298_1588-294dup