Canonical Allele Identifier: CA2631987305
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138168_17138169insTACATCCCTGAAGTTAG , CM000678.2:g.17138168_17138169insTACATCCCTGAAGTTAG GRCh38
NC_000016.9:g.17232025_17232026insTACATCCCTGAAGTTAG , CM000678.1:g.17232025_17232026insTACATCCCTGAAGTTAG GRCh37
NC_000016.8:g.17139526_17139527insTACATCCCTGAAGTTAG NCBI36
NG_015843.1:g.337718_337719insTTCAGGGATGTACTAAC
NG_015843.2:g.337718_337719insTTCAGGGATGTACTAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1764+191_1764+192insTTCAGGGATGTACTAAC MANE Select ENSP00000261381.6:n.1764+191_1764+192insTTCAGGGATGTACTAAC
ENST00000261381.6:c.1764+191_1764+192insTTCAGGGATGTACTAAC ENSP00000261381.6:n.1764+191_1764+192insTTCAGGGATGTACTAAC
NM_022166.3:c.1764+191_1764+192insTTCAGGGATGTACTAAC NP_071449.1:n.1764+191_1764+192insTTCAGGGATGTACTAAC
XM_011522574.1:c.1764+191_1764+192insTTCAGGGATGTACTAAC XP_011520876.1:n.1764+191_1764+192insTTCAGGGATGTACTAAC
XR_933140.1:n.336-74_336-73insTACATCCCTGAAGTTAG
XR_933141.1:n.175-74_175-73insTACATCCCTGAAGTTAG
XR_933143.1:n.237-74_237-73insTACATCCCTGAAGTTAG
NR_135179.1:n.147-74_147-73insTACATCCCTGAAGTTAG
XM_017023539.2:c.1764+191_1764+192insTTCAGGGATGTACTAAC XP_016879028.1:n.1764+191_1764+192insTTCAGGGATGTACTAAC
XM_017023540.2:c.1764+191_1764+192insTTCAGGGATGTACTAAC XP_016879029.1:n.1764+191_1764+192insTTCAGGGATGTACTAAC
NM_022166.4:c.1764+191_1764+192insTTCAGGGATGTACTAAC MANE Select NP_071449.1:n.1764+191_1764+192insTTCAGGGATGTACTAAC