Canonical Allele Identifier: CA2210542157

Gene: XYLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138518G= , CM000678.2:g.17138518G=	GRCh38
NC_000016.9:g.17232375G= , CM000678.1:g.17232375G=	GRCh37
NC_000016.8:g.17139876G=	NCBI36
NG_015843.1:g.337364C=
NG_015843.2:g.337364C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1601C= MANE Select	ENSP00000261381.6:p.Thr534=
ENST00000261381.6:c.1601C=	ENSP00000261381.6:p.Thr534=
NM_022166.3:c.1601C=	NP_071449.1:p.Thr534=
XM_011522574.1:c.1601C=	XP_011520876.1:p.Thr534=
XR_933141.1:n.451G=
NR_135179.1:n.423G=
XM_017023539.2:c.1601C=	XP_016879028.1:p.Thr534=
XM_017023540.2:c.1601C=	XP_016879029.1:p.Thr534=
NM_022166.4:c.1601C= MANE Select	NP_071449.1:p.Thr534=