Canonical Allele Identifier: CA2631987368
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138183_17138184insGAACATCCCTGAAGTG , CM000678.2:g.17138183_17138184insGAACATCCCTGAAGTG GRCh38
NC_000016.9:g.17232040_17232041insGAACATCCCTGAAGTG , CM000678.1:g.17232040_17232041insGAACATCCCTGAAGTG GRCh37
NC_000016.8:g.17139541_17139542insGAACATCCCTGAAGTG NCBI36
NG_015843.1:g.337698_337699insCACTTCAGGGATGTTC
NG_015843.2:g.337698_337699insCACTTCAGGGATGTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1764+171_1764+172insCACTTCAGGGATGTTC MANE Select ENSP00000261381.6:n.1764+171_1764+172insCACTTCAGGGATGTTC
ENST00000261381.6:c.1764+171_1764+172insCACTTCAGGGATGTTC ENSP00000261381.6:n.1764+171_1764+172insCACTTCAGGGATGTTC
NM_022166.3:c.1764+171_1764+172insCACTTCAGGGATGTTC NP_071449.1:n.1764+171_1764+172insCACTTCAGGGATGTTC
XM_011522574.1:c.1764+171_1764+172insCACTTCAGGGATGTTC XP_011520876.1:n.1764+171_1764+172insCACTTCAGGGATGTTC
XR_933140.1:n.336-59_336-58insGAACATCCCTGAAGTG
XR_933141.1:n.175-59_175-58insGAACATCCCTGAAGTG
XR_933143.1:n.237-59_237-58insGAACATCCCTGAAGTG
NR_135179.1:n.147-59_147-58insGAACATCCCTGAAGTG
XM_017023539.2:c.1764+171_1764+172insCACTTCAGGGATGTTC XP_016879028.1:n.1764+171_1764+172insCACTTCAGGGATGTTC
XM_017023540.2:c.1764+171_1764+172insCACTTCAGGGATGTTC XP_016879029.1:n.1764+171_1764+172insCACTTCAGGGATGTTC
NM_022166.4:c.1764+171_1764+172insCACTTCAGGGATGTTC MANE Select NP_071449.1:n.1764+171_1764+172insCACTTCAGGGATGTTC