Canonical Allele Identifier: CA2210542647
Gene: XYLT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138732A= , CM000678.2:g.17138732A= GRCh38
NC_000016.9:g.17232589A= , CM000678.1:g.17232589A= GRCh37
NC_000016.8:g.17140090A= NCBI36
NG_015843.1:g.337150T=
NG_015843.2:g.337150T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1588-201T= MANE Select ENSP00000261381.6:n.1588-201T=
ENST00000261381.6:c.1588-201T= ENSP00000261381.6:n.1588-201T=
NM_022166.3:c.1588-201T= NP_071449.1:n.1588-201T=
XM_011522574.1:c.1588-201T= XP_011520876.1:n.1588-201T=
XR_933141.1:n.665A=
NR_135179.1:n.637A=
XM_017023539.2:c.1588-201T= XP_016879028.1:n.1588-201T=
XM_017023540.2:c.1588-201T= XP_016879029.1:n.1588-201T=
NM_022166.4:c.1588-201T= MANE Select NP_071449.1:n.1588-201T=
Search 100 bp 5'
Search 100 bp 3'