Canonical Allele Identifier: CA2210541522
Gene: XYLT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138178_17138190delinsGAAGTAAGTGCTC , CM000678.2:g.17138178_17138190delinsGAAGTAAGTGCTC GRCh38
NC_000016.9:g.17232035_17232047delinsGAAGTAAGTGCTC , CM000678.1:g.17232035_17232047delinsGAAGTAAGTGCTC GRCh37
NC_000016.8:g.17139536_17139548delinsGAAGTAAGTGCTC NCBI36
NG_015843.1:g.337692_337704delinsGAGCACTTACTTC
NG_015843.2:g.337692_337704delinsGAGCACTTACTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1764+165_1764+177delinsGAGCACTTACTTC MANE Select ENSP00000261381.6:n.1764+165_1764+177delinsGAGCACTTACTTC
ENST00000261381.6:c.1764+165_1764+177delinsGAGCACTTACTTC ENSP00000261381.6:n.1764+165_1764+177delinsGAGCACTTACTTC
NM_022166.3:c.1764+165_1764+177delinsGAGCACTTACTTC NP_071449.1:n.1764+165_1764+177delinsGAGCACTTACTTC
XM_011522574.1:c.1764+165_1764+177delinsGAGCACTTACTTC XP_011520876.1:n.1764+165_1764+177delinsGAGCACTTACTTC
XR_933140.1:n.336-64_336-52delinsGAAGTAAGTGCTC
XR_933141.1:n.175-64_175-52delinsGAAGTAAGTGCTC
XR_933143.1:n.237-64_237-52delinsGAAGTAAGTGCTC
NR_135179.1:n.147-64_147-52delinsGAAGTAAGTGCTC
XM_017023539.2:c.1764+165_1764+177delinsGAGCACTTACTTC XP_016879028.1:n.1764+165_1764+177delinsGAGCACTTACTTC
XM_017023540.2:c.1764+165_1764+177delinsGAGCACTTACTTC XP_016879029.1:n.1764+165_1764+177delinsGAGCACTTACTTC
NM_022166.4:c.1764+165_1764+177delinsGAGCACTTACTTC MANE Select NP_071449.1:n.1764+165_1764+177delinsGAGCACTTACTTC