Canonical Allele Identifier: CA2631986865
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17134603_17134611dup , CM000678.2:g.17134603_17134611dup GRCh38
NC_000016.9:g.17228460_17228468dup , CM000678.1:g.17228460_17228468dup GRCh37
NC_000016.8:g.17135961_17135969dup NCBI36
NG_015843.1:g.341272_341280dup
NG_015843.2:g.341272_341280dup

Transcript Alleles

HGVS Amino-acid change
ENST00000261381.7:c.1890_1898dup MANE Select ENSP00000261381.6:p.Asn633_Val634insTrpGl...
ENST00000261381.6:c.1890_1898dup ENSP00000261381.6:p.Asn633_Val634insTrpGl...
NM_022166.3:c.1890_1898dup NP_071449.1:p.Asn633_Val634insTrpGluAsn
XM_011522574.1:c.1890_1898dup XP_011520876.1:p.Asn633_Val634insTrpGluAs...
XR_933140.1:n.82+53_82+61dup
XR_933141.1:n.75+53_75+61dup
XR_933143.1:n.82+53_82+61dup
NR_135179.1:n.47+53_47+61dup
XM_017023539.2:c.1890_1898dup XP_016879028.1:p.Asn633_Val634insTrpGluAs...
XM_017023540.2:c.1890_1898dup XP_016879029.1:p.Asn633_Val634insTrpGluAs...
NM_022166.4:c.1890_1898dup MANE Select NP_071449.1:p.Asn633_Val634insTrpGluAsn