Canonical Allele Identifier: CA2210543042
Gene: XYLT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17139020T= , CM000678.2:g.17139020T= GRCh38
NC_000016.9:g.17232877T= , CM000678.1:g.17232877T= GRCh37
NC_000016.8:g.17140378T= NCBI36
NG_015843.1:g.336862A=
NG_015843.2:g.336862A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1588-489A= MANE Select ENSP00000261381.6:n.1588-489A=
ENST00000261381.6:c.1588-489A= ENSP00000261381.6:n.1588-489A=
NM_022166.3:c.1588-489A= NP_071449.1:n.1588-489A=
XM_011522574.1:c.1588-489A= XP_011520876.1:n.1588-489A=
XM_017023539.2:c.1588-489A= XP_016879028.1:n.1588-489A=
XM_017023540.2:c.1588-489A= XP_016879029.1:n.1588-489A=
NM_022166.4:c.1588-489A= MANE Select NP_071449.1:n.1588-489A=
Search 100 bp 5'
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