Canonical Allele Identifier: CA494104035

Gene: XYLT1

Linked Data

• MyVariant Identifiers: chr16:g.17228539C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17134682C>T , CM000678.2:g.17134682C>T	GRCh38
NC_000016.9:g.17228539C>T , CM000678.1:g.17228539C>T	GRCh37
NC_000016.8:g.17136040C>T	NCBI36
NG_015843.1:g.341200G>A
NG_015843.2:g.341200G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1818G>A MANE Select	ENSP00000261381.6:p.Gln606=
ENST00000261381.6:c.1818G>A	ENSP00000261381.6:p.Gln606=
NM_022166.3:c.1818G>A	NP_071449.1:p.Gln606=
XM_011522574.1:c.1818G>A	XP_011520876.1:p.Gln606=
XR_933140.1:n.82+132C>T
XR_933141.1:n.75+132C>T
XR_933143.1:n.82+132C>T
NR_135179.1:n.47+132C>T
XM_017023539.2:c.1818G>A	XP_016879028.1:p.Gln606=
XM_017023540.2:c.1818G>A	XP_016879029.1:p.Gln606=
NM_022166.4:c.1818G>A MANE Select	NP_071449.1:p.Gln606=