Canonical Allele Identifier: CA2210542033
Gene: XYLT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138471_17138474delinsGGTT , CM000678.2:g.17138471_17138474delinsGGTT GRCh38
NC_000016.9:g.17232328_17232331delinsGGTT , CM000678.1:g.17232328_17232331delinsGGTT GRCh37
NC_000016.8:g.17139829_17139832delinsGGTT NCBI36
NG_015843.1:g.337408_337411delinsAACC
NG_015843.2:g.337408_337411delinsAACC

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1645_1648delinsAACC MANE Select ENSP00000261381.6:p.Asn549=
ENST00000261381.6:c.1645_1648delinsAACC ENSP00000261381.6:p.Asn549=
NM_022166.3:c.1645_1648delinsAACC NP_071449.1:p.Asn549=
XM_011522574.1:c.1645_1648delinsAACC XP_011520876.1:p.Asn549=
XR_933141.1:n.404_407delinsGGTT
NR_135179.1:n.376_379delinsGGTT
XM_017023539.2:c.1645_1648delinsAACC XP_016879028.1:p.Asn549=
XM_017023540.2:c.1645_1648delinsAACC XP_016879029.1:p.Asn549=
NM_022166.4:c.1645_1648delinsAACC MANE Select NP_071449.1:p.Asn549=
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Search 100 bp 3'