Canonical Allele Identifier: CA395219695
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17134662T>A , CM000678.2:g.17134662T>A GRCh38
NC_000016.9:g.17228519T>A , CM000678.1:g.17228519T>A GRCh37
NC_000016.8:g.17136020T>A NCBI36
NG_015843.1:g.341220A>T
NG_015843.2:g.341220A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1838A>T MANE Select ENSP00000261381.6:p.Asp613Val
ENST00000261381.6:c.1838A>T ENSP00000261381.6:p.Asp613Val
NM_022166.3:c.1838A>T NP_071449.1:p.Asp613Val
XM_011522574.1:c.1838A>T XP_011520876.1:p.Asp613Val
XR_933140.1:n.82+112T>A
XR_933141.1:n.75+112T>A
XR_933143.1:n.82+112T>A
NR_135179.1:n.47+112T>A
XM_017023539.2:c.1838A>T XP_016879028.1:p.Asp613Val
XM_017023540.2:c.1838A>T XP_016879029.1:p.Asp613Val
NM_022166.4:c.1838A>T MANE Select NP_071449.1:p.Asp613Val