Canonical Allele Identifier: CA8646598

Gene: XYLT2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50357234C>T , CM000679.2:g.50357234C>T	GRCh38
NC_000017.10:g.48434595C>T , CM000679.1:g.48434595C>T	GRCh37
NC_000017.9:g.45789594C>T	NCBI36
NG_012175.1:g.16203C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_022167.4:c.1923C>T MANE Select	NP_071450.2:p.Ser641=
ENST00000017003.7:c.1923C>T MANE Select	ENSP00000017003.2:p.Ser641=
NM_022167.3:c.1923C>T	NP_071450.2:p.Ser641=
NR_110010.1:n.1854+461C>T
NR_110010.2:n.1760+461C>T
ENST00000017003.6:c.1923C>T	ENSP00000017003.2:p.Ser641=
ENST00000376550.7:c.1745+461C>T	ENSP00000365733.3:n.1745+461C>T
ENST00000507602.5:c.1923C>T	ENSP00000426501.1:p.Ser641=
ENST00000511654.1:c.458C>T	ENSP00000428350.1:n.458C>T
ENST00000574840.1:c.69C>T	ENSP00000460517.1:p.Ser23=
XM_005257572.3:c.1827C>T	XP_005257629.1:p.Ser609=
XM_005257572.4:c.1827C>T	XP_005257629.1:p.Ser609=
XM_011525114.1:c.1332C>T	XP_011523416.1:p.Ser444=