Canonical Allele Identifier: CA8646305

Gene: XYLT2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50354963G>C , CM000679.2:g.50354963G>C	GRCh38
NC_000017.10:g.48432324G>C , CM000679.1:g.48432324G>C	GRCh37
NC_000017.9:g.45787323G>C	NCBI36
NG_012175.1:g.13932G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000017003.7:c.914G>C MANE Select	ENSP00000017003.2:p.Arg305Thr
ENST00000017003.6:c.914G>C	ENSP00000017003.2:p.Arg305Thr
ENST00000376550.7:c.914G>C	ENSP00000365733.3:p.Arg305Thr
ENST00000507602.5:c.914G>C	ENSP00000426501.1:p.Arg305Thr
NM_022167.3:c.914G>C	NP_071450.2:p.Arg305Thr
NR_110010.1:n.1023G>C
XM_005257572.3:c.818G>C	XP_005257629.1:p.Arg273Thr
XM_011525114.1:c.323G>C	XP_011523416.1:p.Arg108Thr
XM_005257572.4:c.818G>C	XP_005257629.1:p.Arg273Thr
NM_022167.4:c.914G>C MANE Select	NP_071450.2:p.Arg305Thr
NR_110010.2:n.929G>C