Canonical Allele Identifier: CA2631987331
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138177_17138178insCAAGTTAGAACATCCCT , CM000678.2:g.17138177_17138178insCAAGTTAGAACATCCCT GRCh38
NC_000016.9:g.17232034_17232035insCAAGTTAGAACATCCCT , CM000678.1:g.17232034_17232035insCAAGTTAGAACATCCCT GRCh37
NC_000016.8:g.17139535_17139536insCAAGTTAGAACATCCCT NCBI36
NG_015843.1:g.337718_337719insTTGAGGGATGTTCTAAC
NG_015843.2:g.337718_337719insTTGAGGGATGTTCTAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1764+191_1764+192insTTGAGGGATGTTCTAAC MANE Select ENSP00000261381.6:n.1764+191_1764+192insTTGAGGGATGTTCTAAC
ENST00000261381.6:c.1764+191_1764+192insTTGAGGGATGTTCTAAC ENSP00000261381.6:n.1764+191_1764+192insTTGAGGGATGTTCTAAC
NM_022166.3:c.1764+191_1764+192insTTGAGGGATGTTCTAAC NP_071449.1:n.1764+191_1764+192insTTGAGGGATGTTCTAAC
XM_011522574.1:c.1764+191_1764+192insTTGAGGGATGTTCTAAC XP_011520876.1:n.1764+191_1764+192insTTGAGGGATGTTCTAAC
XR_933140.1:n.336-65_336-64insCAAGTTAGAACATCCCT
XR_933141.1:n.175-65_175-64insCAAGTTAGAACATCCCT
XR_933143.1:n.237-65_237-64insCAAGTTAGAACATCCCT
NR_135179.1:n.147-65_147-64insCAAGTTAGAACATCCCT
XM_017023539.2:c.1764+191_1764+192insTTGAGGGATGTTCTAAC XP_016879028.1:n.1764+191_1764+192insTTGAGGGATGTTCTAAC
XM_017023540.2:c.1764+191_1764+192insTTGAGGGATGTTCTAAC XP_016879029.1:n.1764+191_1764+192insTTGAGGGATGTTCTAAC
NM_022166.4:c.1764+191_1764+192insTTGAGGGATGTTCTAAC MANE Select NP_071449.1:n.1764+191_1764+192insTTGAGGGATGTTCTAAC