Canonical Allele Identifier: CA2631987319
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138164_17138165insGTAGAACATCCCTGAAG , CM000678.2:g.17138164_17138165insGTAGAACATCCCTGAAG GRCh38
NC_000016.9:g.17232021_17232022insGTAGAACATCCCTGAAG , CM000678.1:g.17232021_17232022insGTAGAACATCCCTGAAG GRCh37
NC_000016.8:g.17139522_17139523insGTAGAACATCCCTGAAG NCBI36
NG_015843.1:g.337718_337719insTTCAGGGATGTTCTACC
NG_015843.2:g.337718_337719insTTCAGGGATGTTCTACC

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1764+191_1764+192insTTCAGGGATGTTCTACC MANE Select ENSP00000261381.6:n.1764+191_1764+192insTTCAGGGATGTTCTACC
ENST00000261381.6:c.1764+191_1764+192insTTCAGGGATGTTCTACC ENSP00000261381.6:n.1764+191_1764+192insTTCAGGGATGTTCTACC
NM_022166.3:c.1764+191_1764+192insTTCAGGGATGTTCTACC NP_071449.1:n.1764+191_1764+192insTTCAGGGATGTTCTACC
XM_011522574.1:c.1764+191_1764+192insTTCAGGGATGTTCTACC XP_011520876.1:n.1764+191_1764+192insTTCAGGGATGTTCTACC
XR_933140.1:n.336-78_336-77insGTAGAACATCCCTGAAG
XR_933141.1:n.175-78_175-77insGTAGAACATCCCTGAAG
XR_933143.1:n.237-78_237-77insGTAGAACATCCCTGAAG
NR_135179.1:n.147-78_147-77insGTAGAACATCCCTGAAG
XM_017023539.2:c.1764+191_1764+192insTTCAGGGATGTTCTACC XP_016879028.1:n.1764+191_1764+192insTTCAGGGATGTTCTACC
XM_017023540.2:c.1764+191_1764+192insTTCAGGGATGTTCTACC XP_016879029.1:n.1764+191_1764+192insTTCAGGGATGTTCTACC
NM_022166.4:c.1764+191_1764+192insTTCAGGGATGTTCTACC MANE Select NP_071449.1:n.1764+191_1764+192insTTCAGGGATGTTCTACC