Canonical Allele Identifier: CA493798336
Gene: XYLT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.17232420C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138563C>G , CM000678.2:g.17138563C>G GRCh38
NC_000016.9:g.17232420C>G , CM000678.1:g.17232420C>G GRCh37
NC_000016.8:g.17139921C>G NCBI36
NG_015843.1:g.337319G>C
NG_015843.2:g.337319G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1588-32G>C MANE Select ENSP00000261381.6:n.1588-32G>C
ENST00000261381.6:c.1588-32G>C ENSP00000261381.6:n.1588-32G>C
NM_022166.3:c.1588-32G>C NP_071449.1:n.1588-32G>C
XM_011522574.1:c.1588-32G>C XP_011520876.1:n.1588-32G>C
XR_933141.1:n.496C>G
NR_135179.1:n.468C>G
XM_017023539.2:c.1588-32G>C XP_016879028.1:n.1588-32G>C
XM_017023540.2:c.1588-32G>C XP_016879029.1:n.1588-32G>C
NM_022166.4:c.1588-32G>C MANE Select NP_071449.1:n.1588-32G>C