Canonical Allele Identifier: CA395219305
Gene: XYLT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.17228329C>T (hg19) chr16:g.17134472C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17134472C>T , CM000678.2:g.17134472C>T GRCh38
NC_000016.9:g.17228329C>T , CM000678.1:g.17228329C>T GRCh37
NC_000016.8:g.17135830C>T NCBI36
NG_015843.1:g.341410G>A
NG_015843.2:g.341410G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.2027+1G>A MANE Select ENSP00000261381.6:n.2027+1G>A
ENST00000261381.6:c.2027+1G>A ENSP00000261381.6:n.2027+1G>A
NM_022166.3:c.2027+1G>A NP_071449.1:n.2027+1G>A
XM_011522574.1:c.2027+1G>A XP_011520876.1:n.2027+1G>A
XR_933140.1:n.4C>T
XR_933143.1:n.4C>T
XM_017023539.2:c.2027+1G>A XP_016879028.1:n.2027+1G>A
XM_017023540.2:c.2027+1G>A XP_016879029.1:n.2027+1G>A
NM_022166.4:c.2027+1G>A MANE Select NP_071449.1:n.2027+1G>A
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