Canonical Allele Identifier: CA8646483

Gene: XYLT2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50356597T>C , CM000679.2:g.50356597T>C	GRCh38
NC_000017.10:g.48433958T>C , CM000679.1:g.48433958T>C	GRCh37
NC_000017.9:g.45788957T>C	NCBI36
NG_012175.1:g.15566T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000017003.7:c.1569T>C MANE Select	ENSP00000017003.2:p.Tyr523=
ENST00000017003.6:c.1569T>C	ENSP00000017003.2:p.Tyr523=
ENST00000376550.7:c.1569T>C	ENSP00000365733.3:p.Tyr523=
ENST00000507602.5:c.1569T>C	ENSP00000426501.1:p.Tyr523=
ENST00000511654.1:c.165T>C	ENSP00000428350.1:p.Tyr55=
NM_022167.3:c.1569T>C	NP_071450.2:p.Tyr523=
NR_110010.1:n.1678T>C
XM_005257572.3:c.1473T>C	XP_005257629.1:p.Tyr491=
XM_011525114.1:c.978T>C	XP_011523416.1:p.Tyr326=
XM_005257572.4:c.1473T>C	XP_005257629.1:p.Tyr491=
NM_022167.4:c.1569T>C MANE Select	NP_071450.2:p.Tyr523=
NR_110010.2:n.1584T>C