Canonical Allele Identifier: CA2210538841
Gene: XYLT1 HGNC NCBI

Linked Data

dbSNP Id: rs2030645221

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17134749_17134750insGAATGTC , CM000678.2:g.17134749_17134750insGAATGTC GRCh38
NC_000016.9:g.17228606_17228607insGAATGTC , CM000678.1:g.17228606_17228607insGAATGTC GRCh37
NC_000016.8:g.17136107_17136108insGAATGTC NCBI36
NG_015843.1:g.341132_341133insGACATTC
NG_015843.2:g.341132_341133insGACATTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1765-15_1765-14insGACATTC MANE Select ENSP00000261381.6:n.1765-15_1765-14insGACATTC
ENST00000261381.6:c.1765-15_1765-14insGACATTC ENSP00000261381.6:n.1765-15_1765-14insGACATTC
NM_022166.3:c.1765-15_1765-14insGACATTC NP_071449.1:n.1765-15_1765-14insGACATTC
XM_011522574.1:c.1765-15_1765-14insGACATTC XP_011520876.1:n.1765-15_1765-14insGACATTC
XR_933140.1:n.82+199_82+200insGAATGTC
XR_933141.1:n.75+199_75+200insGAATGTC
XR_933143.1:n.82+199_82+200insGAATGTC
NR_135179.1:n.47+199_47+200insGAATGTC
XM_017023539.2:c.1765-15_1765-14insGACATTC XP_016879028.1:n.1765-15_1765-14insGACATTC
XM_017023540.2:c.1765-15_1765-14insGACATTC XP_016879029.1:n.1765-15_1765-14insGACATTC
NM_022166.4:c.1765-15_1765-14insGACATTC MANE Select NP_071449.1:n.1765-15_1765-14insGACATTC