Canonical Allele Identifier: CA2631987487
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138230_17138231insGAACATCCCTGAAGTAAGTGCTCAATAAACACTGGCTATTGTTGATACTGTTAACTATT , CM000678.2:g.17138230_17138231insGAACATCCCTGAAGTAAGTGCTCAATAAACACTGGCTATTGTTGATACTGTTAACTATT GRCh38
NC_000016.9:g.17232087_17232088insGAACATCCCTGAAGTAAGTGCTCAATAAACACTGGCTATTGTTGATACTGTTAACTATT , CM000678.1:g.17232087_17232088insGAACATCCCTGAAGTAAGTGCTCAATAAACACTGGCTATTGTTGATACTGTTAACTATT GRCh37
NC_000016.8:g.17139588_17139589insGAACATCCCTGAAGTAAGTGCTCAATAAACACTGGCTATTGTTGATACTGTTAACTATT NCBI36
NG_015843.1:g.337651_337652insAATAGTTAACAGTATCAACAATAGCCAGTGTTTATTGAGCACTTACTTCAGGGATGTTC
NG_015843.2:g.337651_337652insAATAGTTAACAGTATCAACAATAGCCAGTGTTTATTGAGCACTTACTTCAGGGATGTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1764+124_1764+125insAATAGTTAACAGTATCAACAATAGCCAGTGTTTATTGAGCACTTACTTCAGGGATGTTC MANE Select ENSP00000261381.6:n.1764+124_1764+125insAATAGTTAACAGTATCAACAA...
ENST00000261381.6:c.1764+124_1764+125insAATAGTTAACAGTATCAACAATAGCCAGTGTTTATTGAGCACTTACTTCAGGGATGTTC ENSP00000261381.6:n.1764+124_1764+125insAATAGTTAACAGTATCAACAA...
NM_022166.3:c.1764+124_1764+125insAATAGTTAACAGTATCAACAATAGCCAGTGTTTATTGAGCACTTACTTCAGGGATGTTC NP_071449.1:n.1764+124_1764+125insAATAGTTAACAGTATCAACAATAGCCA...
XM_011522574.1:c.1764+124_1764+125insAATAGTTAACAGTATCAACAATAGCCAGTGTTTATTGAGCACTTACTTCAGGGATGTTC XP_011520876.1:n.1764+124_1764+125insAATAGTTAACAGTATCAACAATAG...
XR_933140.1:n.336-12_336-11insGAACATCCCTGAAGTAAGTGCTCAATAAACACTGGCTATTGTTGATACTGTTAACTATT
XR_933141.1:n.175-12_175-11insGAACATCCCTGAAGTAAGTGCTCAATAAACACTGGCTATTGTTGATACTGTTAACTATT
XR_933143.1:n.237-12_237-11insGAACATCCCTGAAGTAAGTGCTCAATAAACACTGGCTATTGTTGATACTGTTAACTATT
NR_135179.1:n.147-12_147-11insGAACATCCCTGAAGTAAGTGCTCAATAAACACTGGCTATTGTTGATACTGTTAACTATT
XM_017023539.2:c.1764+124_1764+125insAATAGTTAACAGTATCAACAATAGCCAGTGTTTATTGAGCACTTACTTCAGGGATGTTC XP_016879028.1:n.1764+124_1764+125insAATAGTTAACAGTATCAACAATAG...
XM_017023540.2:c.1764+124_1764+125insAATAGTTAACAGTATCAACAATAGCCAGTGTTTATTGAGCACTTACTTCAGGGATGTTC XP_016879029.1:n.1764+124_1764+125insAATAGTTAACAGTATCAACAATAG...
NM_022166.4:c.1764+124_1764+125insAATAGTTAACAGTATCAACAATAGCCAGTGTTTATTGAGCACTTACTTCAGGGATGTTC MANE Select NP_071449.1:n.1764+124_1764+125insAATAGTTAACAGTATCAACAATAGCCA...