Canonical Allele Identifier: CA2631987340
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138182_17138183insTAGAACTTCCCTGAAGT , CM000678.2:g.17138182_17138183insTAGAACTTCCCTGAAGT GRCh38
NC_000016.9:g.17232039_17232040insTAGAACTTCCCTGAAGT , CM000678.1:g.17232039_17232040insTAGAACTTCCCTGAAGT GRCh37
NC_000016.8:g.17139540_17139541insTAGAACTTCCCTGAAGT NCBI36
NG_015843.1:g.337709_337710insAGTTCTAACTTCAGGGA
NG_015843.2:g.337709_337710insAGTTCTAACTTCAGGGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1764+182_1764+183insAGTTCTAACTTCAGGGA MANE Select ENSP00000261381.6:n.1764+182_1764+183insAGTTCTAACTTCAGGGA
ENST00000261381.6:c.1764+182_1764+183insAGTTCTAACTTCAGGGA ENSP00000261381.6:n.1764+182_1764+183insAGTTCTAACTTCAGGGA
NM_022166.3:c.1764+182_1764+183insAGTTCTAACTTCAGGGA NP_071449.1:n.1764+182_1764+183insAGTTCTAACTTCAGGGA
XM_011522574.1:c.1764+182_1764+183insAGTTCTAACTTCAGGGA XP_011520876.1:n.1764+182_1764+183insAGTTCTAACTTCAGGGA
XR_933140.1:n.336-60_336-59insTAGAACTTCCCTGAAGT
XR_933141.1:n.175-60_175-59insTAGAACTTCCCTGAAGT
XR_933143.1:n.237-60_237-59insTAGAACTTCCCTGAAGT
NR_135179.1:n.147-60_147-59insTAGAACTTCCCTGAAGT
XM_017023539.2:c.1764+182_1764+183insAGTTCTAACTTCAGGGA XP_016879028.1:n.1764+182_1764+183insAGTTCTAACTTCAGGGA
XM_017023540.2:c.1764+182_1764+183insAGTTCTAACTTCAGGGA XP_016879029.1:n.1764+182_1764+183insAGTTCTAACTTCAGGGA
NM_022166.4:c.1764+182_1764+183insAGTTCTAACTTCAGGGA MANE Select NP_071449.1:n.1764+182_1764+183insAGTTCTAACTTCAGGGA