Canonical Allele Identifier: CA394876773

Gene: XYLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17141230C>A , CM000678.2:g.17141230C>A	GRCh38
NC_000016.9:g.17235087C>A , CM000678.1:g.17235087C>A	GRCh37
NC_000016.8:g.17142588C>A	NCBI36
NG_015843.1:g.334652G>T
NG_015843.2:g.334652G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_022166.4:c.1510G>T MANE Select	NP_071449.1:p.Glu504Ter
ENST00000261381.7:c.1510G>T MANE Select	ENSP00000261381.6:p.Glu504Ter
NM_022166.3:c.1510G>T	NP_071449.1:p.Glu504Ter
ENST00000261381.6:c.1510G>T	ENSP00000261381.6:p.Glu504Ter
XM_011522574.1:c.1510G>T	XP_011520876.1:p.Glu504Ter
XM_017023539.2:c.1510G>T	XP_016879028.1:p.Glu504Ter
XM_017023540.2:c.1510G>T	XP_016879029.1:p.Glu504Ter