Canonical Allele Identifier: CA2631987325
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138172_17138173insACCCTGAAGTTAGAACA , CM000678.2:g.17138172_17138173insACCCTGAAGTTAGAACA GRCh38
NC_000016.9:g.17232029_17232030insACCCTGAAGTTAGAACA , CM000678.1:g.17232029_17232030insACCCTGAAGTTAGAACA GRCh37
NC_000016.8:g.17139530_17139531insACCCTGAAGTTAGAACA NCBI36
NG_015843.1:g.337718_337719insTTCAGGGTTGTTCTAAC
NG_015843.2:g.337718_337719insTTCAGGGTTGTTCTAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1764+191_1764+192insTTCAGGGTTGTTCTAAC MANE Select ENSP00000261381.6:n.1764+191_1764+192insTTCAGGGTTGTTCTAAC
ENST00000261381.6:c.1764+191_1764+192insTTCAGGGTTGTTCTAAC ENSP00000261381.6:n.1764+191_1764+192insTTCAGGGTTGTTCTAAC
NM_022166.3:c.1764+191_1764+192insTTCAGGGTTGTTCTAAC NP_071449.1:n.1764+191_1764+192insTTCAGGGTTGTTCTAAC
XM_011522574.1:c.1764+191_1764+192insTTCAGGGTTGTTCTAAC XP_011520876.1:n.1764+191_1764+192insTTCAGGGTTGTTCTAAC
XR_933140.1:n.336-70_336-69insACCCTGAAGTTAGAACA
XR_933141.1:n.175-70_175-69insACCCTGAAGTTAGAACA
XR_933143.1:n.237-70_237-69insACCCTGAAGTTAGAACA
NR_135179.1:n.147-70_147-69insACCCTGAAGTTAGAACA
XM_017023539.2:c.1764+191_1764+192insTTCAGGGTTGTTCTAAC XP_016879028.1:n.1764+191_1764+192insTTCAGGGTTGTTCTAAC
XM_017023540.2:c.1764+191_1764+192insTTCAGGGTTGTTCTAAC XP_016879029.1:n.1764+191_1764+192insTTCAGGGTTGTTCTAAC
NM_022166.4:c.1764+191_1764+192insTTCAGGGTTGTTCTAAC MANE Select NP_071449.1:n.1764+191_1764+192insTTCAGGGTTGTTCTAAC