Canonical Allele Identifier: CA2210538819

Gene: XYLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17134707C= , CM000678.2:g.17134707C=	GRCh38
NC_000016.9:g.17228564C= , CM000678.1:g.17228564C=	GRCh37
NC_000016.8:g.17136065C=	NCBI36
NG_015843.1:g.341175G=
NG_015843.2:g.341175G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1793G= MANE Select	ENSP00000261381.6:p.Arg598=
ENST00000261381.6:c.1793G=	ENSP00000261381.6:p.Arg598=
NM_022166.3:c.1793G=	NP_071449.1:p.Arg598=
XM_011522574.1:c.1793G=	XP_011520876.1:p.Arg598=
XR_933140.1:n.82+157C=
XR_933141.1:n.75+157C=
XR_933143.1:n.82+157C=
NR_135179.1:n.47+157C=
XM_017023539.2:c.1793G=	XP_016879028.1:p.Arg598=
XM_017023540.2:c.1793G=	XP_016879029.1:p.Arg598=
NM_022166.4:c.1793G= MANE Select	NP_071449.1:p.Arg598=