Canonical Allele Identifier: CA2631987611
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138698_17138699insACA , CM000678.2:g.17138698_17138699insACA GRCh38
NC_000016.9:g.17232555_17232556insACA , CM000678.1:g.17232555_17232556insACA GRCh37
NC_000016.8:g.17140056_17140057insACA NCBI36
NG_015843.1:g.337183_337184insTGT
NG_015843.2:g.337183_337184insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1588-168_1588-167insTGT MANE Select ENSP00000261381.6:n.1588-168_1588-167insTGT
ENST00000261381.6:c.1588-168_1588-167insTGT ENSP00000261381.6:n.1588-168_1588-167insTGT
NM_022166.3:c.1588-168_1588-167insTGT NP_071449.1:n.1588-168_1588-167insTGT
XM_011522574.1:c.1588-168_1588-167insTGT XP_011520876.1:n.1588-168_1588-167insTGT
XR_933141.1:n.631_632insACA
NR_135179.1:n.603_604insACA
XM_017023539.2:c.1588-168_1588-167insTGT XP_016879028.1:n.1588-168_1588-167insTGT
XM_017023540.2:c.1588-168_1588-167insTGT XP_016879029.1:n.1588-168_1588-167insTGT
NM_022166.4:c.1588-168_1588-167insTGT MANE Select NP_071449.1:n.1588-168_1588-167insTGT