Canonical Allele Identifier: CA2631987295
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138171_17138172insCTCCCTGAAGTTAGAAC , CM000678.2:g.17138171_17138172insCTCCCTGAAGTTAGAAC GRCh38
NC_000016.9:g.17232028_17232029insCTCCCTGAAGTTAGAAC , CM000678.1:g.17232028_17232029insCTCCCTGAAGTTAGAAC GRCh37
NC_000016.8:g.17139529_17139530insCTCCCTGAAGTTAGAAC NCBI36
NG_015843.1:g.337718_337719insTTCAGGGAGGTTCTAAC
NG_015843.2:g.337718_337719insTTCAGGGAGGTTCTAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1764+191_1764+192insTTCAGGGAGGTTCTAAC MANE Select ENSP00000261381.6:n.1764+191_1764+192insTTCAGGGAGGTTCTAAC
ENST00000261381.6:c.1764+191_1764+192insTTCAGGGAGGTTCTAAC ENSP00000261381.6:n.1764+191_1764+192insTTCAGGGAGGTTCTAAC
NM_022166.3:c.1764+191_1764+192insTTCAGGGAGGTTCTAAC NP_071449.1:n.1764+191_1764+192insTTCAGGGAGGTTCTAAC
XM_011522574.1:c.1764+191_1764+192insTTCAGGGAGGTTCTAAC XP_011520876.1:n.1764+191_1764+192insTTCAGGGAGGTTCTAAC
XR_933140.1:n.336-71_336-70insCTCCCTGAAGTTAGAAC
XR_933141.1:n.175-71_175-70insCTCCCTGAAGTTAGAAC
XR_933143.1:n.237-71_237-70insCTCCCTGAAGTTAGAAC
NR_135179.1:n.147-71_147-70insCTCCCTGAAGTTAGAAC
XM_017023539.2:c.1764+191_1764+192insTTCAGGGAGGTTCTAAC XP_016879028.1:n.1764+191_1764+192insTTCAGGGAGGTTCTAAC
XM_017023540.2:c.1764+191_1764+192insTTCAGGGAGGTTCTAAC XP_016879029.1:n.1764+191_1764+192insTTCAGGGAGGTTCTAAC
NM_022166.4:c.1764+191_1764+192insTTCAGGGAGGTTCTAAC MANE Select NP_071449.1:n.1764+191_1764+192insTTCAGGGAGGTTCTAAC