Canonical Allele Identifier: CA2210542162
Gene: XYLT1 HGNC NCBI

Linked Data

dbSNP Id: rs2030851210

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138521_17138544dup , CM000678.2:g.17138521_17138544dup GRCh38
NC_000016.9:g.17232378_17232401dup , CM000678.1:g.17232378_17232401dup GRCh37
NC_000016.8:g.17139879_17139902dup NCBI36
NG_015843.1:g.337338_337361dup
NG_015843.2:g.337338_337361dup

Transcript Alleles

HGVS Amino-acid change
ENST00000261381.7:c.1588-13_1598dup
ENST00000261381.6:c.1588-13_1598dup
NM_022166.3:c.1588-13_1598dup
XM_011522574.1:c.1588-13_1598dup
XR_933141.1:n.454_477dup
NR_135179.1:n.426_449dup
XM_017023539.2:c.1588-13_1598dup
XM_017023540.2:c.1588-13_1598dup
NM_022166.4:c.1588-13_1598dup