Canonical Allele Identifier: CA14405723

Gene: XYLT2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50354709A>G , CM000679.2:g.50354709A>G	GRCh38
NC_000017.10:g.48432070A>G , CM000679.1:g.48432070A>G	GRCh37
NC_000017.9:g.45787069A>G	NCBI36
NG_012175.1:g.13678A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_022167.4:c.804+126A>G MANE Select	NP_071450.2:n.804+126A>G
ENST00000017003.7:c.804+126A>G MANE Select	ENSP00000017003.2:n.804+126A>G
NM_022167.3:c.804+126A>G	NP_071450.2:n.804+126A>G
NR_110010.1:n.913+126A>G
NR_110010.2:n.819+126A>G
ENST00000017003.6:c.804+126A>G	ENSP00000017003.2:n.804+126A>G
ENST00000376550.7:c.804+126A>G	ENSP00000365733.3:n.804+126A>G
ENST00000507602.5:c.804+126A>G	ENSP00000426501.1:n.804+126A>G
XM_005257572.3:c.708+126A>G	XP_005257629.1:n.708+126A>G
XM_005257572.4:c.708+126A>G	XP_005257629.1:n.708+126A>G
XM_011525114.1:c.213+126A>G	XP_011523416.1:n.213+126A>G