Canonical Allele Identifier: CA2631987328
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138173_17138174insACCTGAAGTTAGAACAT , CM000678.2:g.17138173_17138174insACCTGAAGTTAGAACAT GRCh38
NC_000016.9:g.17232030_17232031insACCTGAAGTTAGAACAT , CM000678.1:g.17232030_17232031insACCTGAAGTTAGAACAT GRCh37
NC_000016.8:g.17139531_17139532insACCTGAAGTTAGAACAT NCBI36
NG_015843.1:g.337718_337719insTTCAGGTATGTTCTAAC
NG_015843.2:g.337718_337719insTTCAGGTATGTTCTAAC

Transcript Alleles

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