Canonical Allele Identifier: CA2210538855
Gene: XYLT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17134778_17134785delinsTGCTGGGG , CM000678.2:g.17134778_17134785delinsTGCTGGGG GRCh38
NC_000016.9:g.17228635_17228642delinsTGCTGGGG , CM000678.1:g.17228635_17228642delinsTGCTGGGG GRCh37
NC_000016.8:g.17136136_17136143delinsTGCTGGGG NCBI36
NG_015843.1:g.341097_341104delinsCCCCAGCA
NG_015843.2:g.341097_341104delinsCCCCAGCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1765-50_1765-43delinsCCCCAGCA MANE Select ENSP00000261381.6:n.1765-50_1765-43delinsCCCCAGCA
ENST00000261381.6:c.1765-50_1765-43delinsCCCCAGCA ENSP00000261381.6:n.1765-50_1765-43delinsCCCCAGCA
NM_022166.3:c.1765-50_1765-43delinsCCCCAGCA NP_071449.1:n.1765-50_1765-43delinsCCCCAGCA
XM_011522574.1:c.1765-50_1765-43delinsCCCCAGCA XP_011520876.1:n.1765-50_1765-43delinsCCCCAGCA
XR_933140.1:n.82+228_82+235delinsTGCTGGGG
XR_933141.1:n.75+228_75+235delinsTGCTGGGG
XR_933143.1:n.82+228_82+235delinsTGCTGGGG
NR_135179.1:n.47+228_47+235delinsTGCTGGGG
XM_017023539.2:c.1765-50_1765-43delinsCCCCAGCA XP_016879028.1:n.1765-50_1765-43delinsCCCCAGCA
XM_017023540.2:c.1765-50_1765-43delinsCCCCAGCA XP_016879029.1:n.1765-50_1765-43delinsCCCCAGCA
NM_022166.4:c.1765-50_1765-43delinsCCCCAGCA MANE Select NP_071449.1:n.1765-50_1765-43delinsCCCCAGCA