Canonical Allele Identifier: CA394875172
Gene: XYLT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.17232245A>C (hg19) chr16:g.17138388A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138388A>C , CM000678.2:g.17138388A>C GRCh38
NC_000016.9:g.17232245A>C , CM000678.1:g.17232245A>C GRCh37
NC_000016.8:g.17139746A>C NCBI36
NG_015843.1:g.337494T>G
NG_015843.2:g.337494T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1731T>G MANE Select ENSP00000261381.6:p.Asn577Lys
ENST00000261381.6:c.1731T>G ENSP00000261381.6:p.Asn577Lys
NM_022166.3:c.1731T>G NP_071449.1:p.Asn577Lys
XM_011522574.1:c.1731T>G XP_011520876.1:p.Asn577Lys
XR_933141.1:n.321A>C
NR_135179.1:n.293A>C
XM_017023539.2:c.1731T>G XP_016879028.1:p.Asn577Lys
XM_017023540.2:c.1731T>G XP_016879029.1:p.Asn577Lys
NM_022166.4:c.1731T>G MANE Select NP_071449.1:p.Asn577Lys
Search 100 bp 5'
Search 100 bp 3'