Canonical Allele Identifier: CA2631987316
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138163_17138164insCTTAGAACATCCCTGAA , CM000678.2:g.17138163_17138164insCTTAGAACATCCCTGAA GRCh38
NC_000016.9:g.17232020_17232021insCTTAGAACATCCCTGAA , CM000678.1:g.17232020_17232021insCTTAGAACATCCCTGAA GRCh37
NC_000016.8:g.17139521_17139522insCTTAGAACATCCCTGAA NCBI36
NG_015843.1:g.337718_337719insTTCAGGGATGTTCTAAG
NG_015843.2:g.337718_337719insTTCAGGGATGTTCTAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1764+191_1764+192insTTCAGGGATGTTCTAAG MANE Select ENSP00000261381.6:n.1764+191_1764+192insTTCAGGGATGTTCTAAG
ENST00000261381.6:c.1764+191_1764+192insTTCAGGGATGTTCTAAG ENSP00000261381.6:n.1764+191_1764+192insTTCAGGGATGTTCTAAG
NM_022166.3:c.1764+191_1764+192insTTCAGGGATGTTCTAAG NP_071449.1:n.1764+191_1764+192insTTCAGGGATGTTCTAAG
XM_011522574.1:c.1764+191_1764+192insTTCAGGGATGTTCTAAG XP_011520876.1:n.1764+191_1764+192insTTCAGGGATGTTCTAAG
XR_933140.1:n.336-79_336-78insCTTAGAACATCCCTGAA
XR_933141.1:n.175-79_175-78insCTTAGAACATCCCTGAA
XR_933143.1:n.237-79_237-78insCTTAGAACATCCCTGAA
NR_135179.1:n.147-79_147-78insCTTAGAACATCCCTGAA
XM_017023539.2:c.1764+191_1764+192insTTCAGGGATGTTCTAAG XP_016879028.1:n.1764+191_1764+192insTTCAGGGATGTTCTAAG
XM_017023540.2:c.1764+191_1764+192insTTCAGGGATGTTCTAAG XP_016879029.1:n.1764+191_1764+192insTTCAGGGATGTTCTAAG
NM_022166.4:c.1764+191_1764+192insTTCAGGGATGTTCTAAG MANE Select NP_071449.1:n.1764+191_1764+192insTTCAGGGATGTTCTAAG