Canonical Allele Identifier: CA2210541602

Gene: XYLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138229T= , CM000678.2:g.17138229T=	GRCh38
NC_000016.9:g.17232086T= , CM000678.1:g.17232086T=	GRCh37
NC_000016.8:g.17139587T=	NCBI36
NG_015843.1:g.337653A=
NG_015843.2:g.337653A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+126A= MANE Select	ENSP00000261381.6:n.1764+126A=
ENST00000261381.6:c.1764+126A=	ENSP00000261381.6:n.1764+126A=
NM_022166.3:c.1764+126A=	NP_071449.1:n.1764+126A=
XM_011522574.1:c.1764+126A=	XP_011520876.1:n.1764+126A=
XR_933140.1:n.336-13T=
XR_933141.1:n.175-13T=
XR_933143.1:n.237-13T=
NR_135179.1:n.147-13T=
XM_017023539.2:c.1764+126A=	XP_016879028.1:n.1764+126A=
XM_017023540.2:c.1764+126A=	XP_016879029.1:n.1764+126A=
NM_022166.4:c.1764+126A= MANE Select	NP_071449.1:n.1764+126A=