Canonical Allele Identifier: CA2210542990
Gene: XYLT1 HGNC NCBI

Linked Data

dbSNP Id: rs2030876427
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138991C>T , CM000678.2:g.17138991C>T GRCh38
NC_000016.9:g.17232848C>T , CM000678.1:g.17232848C>T GRCh37
NC_000016.8:g.17140349C>T NCBI36
NG_015843.1:g.336891G>A
NG_015843.2:g.336891G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1588-460G>A MANE Select ENSP00000261381.6:n.1588-460G>A
ENST00000261381.6:c.1588-460G>A ENSP00000261381.6:n.1588-460G>A
NM_022166.3:c.1588-460G>A NP_071449.1:n.1588-460G>A
XM_011522574.1:c.1588-460G>A XP_011520876.1:n.1588-460G>A
XM_017023539.2:c.1588-460G>A XP_016879028.1:n.1588-460G>A
XM_017023540.2:c.1588-460G>A XP_016879029.1:n.1588-460G>A
NM_022166.4:c.1588-460G>A MANE Select NP_071449.1:n.1588-460G>A
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