Canonical Allele Identifier: CA2631987356
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138182_17138183insTAGAACATCCCTAAAGT , CM000678.2:g.17138182_17138183insTAGAACATCCCTAAAGT GRCh38
NC_000016.9:g.17232039_17232040insTAGAACATCCCTAAAGT , CM000678.1:g.17232039_17232040insTAGAACATCCCTAAAGT GRCh37
NC_000016.8:g.17139540_17139541insTAGAACATCCCTAAAGT NCBI36
NG_015843.1:g.337703_337704insTAGGGATGTTCTAACTT
NG_015843.2:g.337703_337704insTAGGGATGTTCTAACTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1764+176_1764+177insTAGGGATGTTCTAACTT MANE Select ENSP00000261381.6:n.1764+176_1764+177insTAGGGATGTTCTAACTT
ENST00000261381.6:c.1764+176_1764+177insTAGGGATGTTCTAACTT ENSP00000261381.6:n.1764+176_1764+177insTAGGGATGTTCTAACTT
NM_022166.3:c.1764+176_1764+177insTAGGGATGTTCTAACTT NP_071449.1:n.1764+176_1764+177insTAGGGATGTTCTAACTT
XM_011522574.1:c.1764+176_1764+177insTAGGGATGTTCTAACTT XP_011520876.1:n.1764+176_1764+177insTAGGGATGTTCTAACTT
XR_933140.1:n.336-60_336-59insTAGAACATCCCTAAAGT
XR_933141.1:n.175-60_175-59insTAGAACATCCCTAAAGT
XR_933143.1:n.237-60_237-59insTAGAACATCCCTAAAGT
NR_135179.1:n.147-60_147-59insTAGAACATCCCTAAAGT
XM_017023539.2:c.1764+176_1764+177insTAGGGATGTTCTAACTT XP_016879028.1:n.1764+176_1764+177insTAGGGATGTTCTAACTT
XM_017023540.2:c.1764+176_1764+177insTAGGGATGTTCTAACTT XP_016879029.1:n.1764+176_1764+177insTAGGGATGTTCTAACTT
NM_022166.4:c.1764+176_1764+177insTAGGGATGTTCTAACTT MANE Select NP_071449.1:n.1764+176_1764+177insTAGGGATGTTCTAACTT