Canonical Allele Identifier: CA2631987427
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138207_17138208insAATGAGTCAATGTGGTTAGAACATCCCTGAAGTAA , CM000678.2:g.17138207_17138208insAATGAGTCAATGTGGTTAGAACATCCCTGAAGTAA GRCh38
NC_000016.9:g.17232064_17232065insAATGAGTCAATGTGGTTAGAACATCCCTGAAGTAA , CM000678.1:g.17232064_17232065insAATGAGTCAATGTGGTTAGAACATCCCTGAAGTAA GRCh37
NC_000016.8:g.17139565_17139566insAATGAGTCAATGTGGTTAGAACATCCCTGAAGTAA NCBI36
NG_015843.1:g.337674_337675insTTACTTCAGGGATGTTCTAACCACATTGACTCATT
NG_015843.2:g.337674_337675insTTACTTCAGGGATGTTCTAACCACATTGACTCATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1764+147_1764+148insTTACTTCAGGGATGTTCTAACCACATTGACTCATT MANE Select ENSP00000261381.6:n.1764+147_1764+148insTTACTTCAGGGATGTTCTAAC...
ENST00000261381.6:c.1764+147_1764+148insTTACTTCAGGGATGTTCTAACCACATTGACTCATT ENSP00000261381.6:n.1764+147_1764+148insTTACTTCAGGGATGTTCTAAC...
NM_022166.3:c.1764+147_1764+148insTTACTTCAGGGATGTTCTAACCACATTGACTCATT NP_071449.1:n.1764+147_1764+148insTTACTTCAGGGATGTTCTAACCACATT...
XM_011522574.1:c.1764+147_1764+148insTTACTTCAGGGATGTTCTAACCACATTGACTCATT XP_011520876.1:n.1764+147_1764+148insTTACTTCAGGGATGTTCTAACCAC...
XR_933140.1:n.336-35_336-34insAATGAGTCAATGTGGTTAGAACATCCCTGAAGTAA
XR_933141.1:n.175-35_175-34insAATGAGTCAATGTGGTTAGAACATCCCTGAAGTAA
XR_933143.1:n.237-35_237-34insAATGAGTCAATGTGGTTAGAACATCCCTGAAGTAA
NR_135179.1:n.147-35_147-34insAATGAGTCAATGTGGTTAGAACATCCCTGAAGTAA
XM_017023539.2:c.1764+147_1764+148insTTACTTCAGGGATGTTCTAACCACATTGACTCATT XP_016879028.1:n.1764+147_1764+148insTTACTTCAGGGATGTTCTAACCAC...
XM_017023540.2:c.1764+147_1764+148insTTACTTCAGGGATGTTCTAACCACATTGACTCATT XP_016879029.1:n.1764+147_1764+148insTTACTTCAGGGATGTTCTAACCAC...
NM_022166.4:c.1764+147_1764+148insTTACTTCAGGGATGTTCTAACCACATTGACTCATT MANE Select NP_071449.1:n.1764+147_1764+148insTTACTTCAGGGATGTTCTAACCACATT...