Canonical Allele Identifier: CA7927752
Gene: XYLT1 HGNC NCBI

Linked Data

dbSNP Id: rs777372481
ExAC: 16:17228514 A / T
gnomAD v2: 16-17228514-A-T
gnomAD v3: 16-17134657-A-T
gnomAD v4: 16-17134657-A-T
MyVariant Identifiers: chr16:g.17228514A>T (hg19) chr16:g.17134657A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17134657A>T , CM000678.2:g.17134657A>T GRCh38
NC_000016.9:g.17228514A>T , CM000678.1:g.17228514A>T GRCh37
NC_000016.8:g.17136015A>T NCBI36
NG_015843.1:g.341225T>A
NG_015843.2:g.341225T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1843T>A MANE Select ENSP00000261381.6:p.Tyr615Asn
ENST00000261381.6:c.1843T>A ENSP00000261381.6:p.Tyr615Asn
NM_022166.3:c.1843T>A NP_071449.1:p.Tyr615Asn
XM_011522574.1:c.1843T>A XP_011520876.1:p.Tyr615Asn
XR_933140.1:n.82+107A>T
XR_933141.1:n.75+107A>T
XR_933143.1:n.82+107A>T
NR_135179.1:n.47+107A>T
XM_017023539.2:c.1843T>A XP_016879028.1:p.Tyr615Asn
XM_017023540.2:c.1843T>A XP_016879029.1:p.Tyr615Asn
NM_022166.4:c.1843T>A MANE Select NP_071449.1:p.Tyr615Asn
Search 100 bp 5'
Search 100 bp 3'