Canonical Allele Identifier: CA394875127
Gene: XYLT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.17232226A>G (hg19) chr16:g.17138369A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138369A>G , CM000678.2:g.17138369A>G GRCh38
NC_000016.9:g.17232226A>G , CM000678.1:g.17232226A>G GRCh37
NC_000016.8:g.17139727A>G NCBI36
NG_015843.1:g.337513T>C
NG_015843.2:g.337513T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1750T>C MANE Select ENSP00000261381.6:p.Phe584Leu
ENST00000261381.6:c.1750T>C ENSP00000261381.6:p.Phe584Leu
NM_022166.3:c.1750T>C NP_071449.1:p.Phe584Leu
XM_011522574.1:c.1750T>C XP_011520876.1:p.Phe584Leu
XR_933141.1:n.302A>G
NR_135179.1:n.274A>G
XM_017023539.2:c.1750T>C XP_016879028.1:p.Phe584Leu
XM_017023540.2:c.1750T>C XP_016879029.1:p.Phe584Leu
NM_022166.4:c.1750T>C MANE Select NP_071449.1:p.Phe584Leu
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