Canonical Allele Identifier: CA2631987372
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138184_17138185insCATCCCTGAAGTAG , CM000678.2:g.17138184_17138185insCATCCCTGAAGTAG GRCh38
NC_000016.9:g.17232041_17232042insCATCCCTGAAGTAG , CM000678.1:g.17232041_17232042insCATCCCTGAAGTAG GRCh37
NC_000016.8:g.17139542_17139543insCATCCCTGAAGTAG NCBI36
NG_015843.1:g.337697_337698insCTACTTCAGGGATG
NG_015843.2:g.337697_337698insCTACTTCAGGGATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1764+170_1764+171insCTACTTCAGGGATG MANE Select ENSP00000261381.6:n.1764+170_1764+171insCTACTTCAGGGATG
ENST00000261381.6:c.1764+170_1764+171insCTACTTCAGGGATG ENSP00000261381.6:n.1764+170_1764+171insCTACTTCAGGGATG
NM_022166.3:c.1764+170_1764+171insCTACTTCAGGGATG NP_071449.1:n.1764+170_1764+171insCTACTTCAGGGATG
XM_011522574.1:c.1764+170_1764+171insCTACTTCAGGGATG XP_011520876.1:n.1764+170_1764+171insCTACTTCAGGGATG
XR_933140.1:n.336-58_336-57insCATCCCTGAAGTAG
XR_933141.1:n.175-58_175-57insCATCCCTGAAGTAG
XR_933143.1:n.237-58_237-57insCATCCCTGAAGTAG
NR_135179.1:n.147-58_147-57insCATCCCTGAAGTAG
XM_017023539.2:c.1764+170_1764+171insCTACTTCAGGGATG XP_016879028.1:n.1764+170_1764+171insCTACTTCAGGGATG
XM_017023540.2:c.1764+170_1764+171insCTACTTCAGGGATG XP_016879029.1:n.1764+170_1764+171insCTACTTCAGGGATG
NM_022166.4:c.1764+170_1764+171insCTACTTCAGGGATG MANE Select NP_071449.1:n.1764+170_1764+171insCTACTTCAGGGATG