Canonical Allele Identifier: CA395219317
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17134477A>T , CM000678.2:g.17134477A>T GRCh38
NC_000016.9:g.17228334A>T , CM000678.1:g.17228334A>T GRCh37
NC_000016.8:g.17135835A>T NCBI36
NG_015843.1:g.341405T>A
NG_015843.2:g.341405T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.2023T>A MANE Select ENSP00000261381.6:p.Cys675Ser
ENST00000261381.6:c.2023T>A ENSP00000261381.6:p.Cys675Ser
NM_022166.3:c.2023T>A NP_071449.1:p.Cys675Ser
XM_011522574.1:c.2023T>A XP_011520876.1:p.Cys675Ser
XR_933140.1:n.9A>T
XR_933141.1:n.2A>T
XR_933143.1:n.9A>T
XM_017023539.2:c.2023T>A XP_016879028.1:p.Cys675Ser
XM_017023540.2:c.2023T>A XP_016879029.1:p.Cys675Ser
NM_022166.4:c.2023T>A MANE Select NP_071449.1:p.Cys675Ser