Canonical Allele Identifier: CA494103902

Gene: XYLT1

Linked Data

• MyVariant Identifiers: chr16:g.17228494A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17134637A>T , CM000678.2:g.17134637A>T	GRCh38
NC_000016.9:g.17228494A>T , CM000678.1:g.17228494A>T	GRCh37
NC_000016.8:g.17135995A>T	NCBI36
NG_015843.1:g.341245T>A
NG_015843.2:g.341245T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1863T>A MANE Select	ENSP00000261381.6:p.Pro621=
ENST00000261381.6:c.1863T>A	ENSP00000261381.6:p.Pro621=
NM_022166.3:c.1863T>A	NP_071449.1:p.Pro621=
XM_011522574.1:c.1863T>A	XP_011520876.1:p.Pro621=
XR_933140.1:n.82+87A>T
XR_933141.1:n.75+87A>T
XR_933143.1:n.82+87A>T
NR_135179.1:n.47+87A>T
XM_017023539.2:c.1863T>A	XP_016879028.1:p.Pro621=
XM_017023540.2:c.1863T>A	XP_016879029.1:p.Pro621=
NM_022166.4:c.1863T>A MANE Select	NP_071449.1:p.Pro621=