Canonical Allele Identifier: CA2631987294
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138173_17138174insGCCTGAAGTTAGAACAT , CM000678.2:g.17138173_17138174insGCCTGAAGTTAGAACAT GRCh38
NC_000016.9:g.17232030_17232031insGCCTGAAGTTAGAACAT , CM000678.1:g.17232030_17232031insGCCTGAAGTTAGAACAT GRCh37
NC_000016.8:g.17139531_17139532insGCCTGAAGTTAGAACAT NCBI36
NG_015843.1:g.337718_337719insTTCAGGCATGTTCTAAC
NG_015843.2:g.337718_337719insTTCAGGCATGTTCTAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1764+191_1764+192insTTCAGGCATGTTCTAAC MANE Select ENSP00000261381.6:n.1764+191_1764+192insTTCAGGCATGTTCTAAC
ENST00000261381.6:c.1764+191_1764+192insTTCAGGCATGTTCTAAC ENSP00000261381.6:n.1764+191_1764+192insTTCAGGCATGTTCTAAC
NM_022166.3:c.1764+191_1764+192insTTCAGGCATGTTCTAAC NP_071449.1:n.1764+191_1764+192insTTCAGGCATGTTCTAAC
XM_011522574.1:c.1764+191_1764+192insTTCAGGCATGTTCTAAC XP_011520876.1:n.1764+191_1764+192insTTCAGGCATGTTCTAAC
XR_933140.1:n.336-69_336-68insGCCTGAAGTTAGAACAT
XR_933141.1:n.175-69_175-68insGCCTGAAGTTAGAACAT
XR_933143.1:n.237-69_237-68insGCCTGAAGTTAGAACAT
NR_135179.1:n.147-69_147-68insGCCTGAAGTTAGAACAT
XM_017023539.2:c.1764+191_1764+192insTTCAGGCATGTTCTAAC XP_016879028.1:n.1764+191_1764+192insTTCAGGCATGTTCTAAC
XM_017023540.2:c.1764+191_1764+192insTTCAGGCATGTTCTAAC XP_016879029.1:n.1764+191_1764+192insTTCAGGCATGTTCTAAC
NM_022166.4:c.1764+191_1764+192insTTCAGGCATGTTCTAAC MANE Select NP_071449.1:n.1764+191_1764+192insTTCAGGCATGTTCTAAC