Canonical Allele Identifier: CA2806078123

Gene: XYLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138533_17138534insTCCACC , CM000678.2:g.17138533_17138534insTCCACC	GRCh38
NC_000016.9:g.17232390_17232391insTCCACC , CM000678.1:g.17232390_17232391insTCCACC	GRCh37
NC_000016.8:g.17139891_17139892insTCCACC	NCBI36
NG_015843.1:g.337348_337349insGGTGGA
NG_015843.2:g.337348_337349insGGTGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-3_1588-2insGGTGGA MANE Select	ENSP00000261381.6:n.1588-3_1588-2insGGTGGA
ENST00000261381.6:c.1588-3_1588-2insGGTGGA	ENSP00000261381.6:n.1588-3_1588-2insGGTGGA
NM_022166.3:c.1588-3_1588-2insGGTGGA	NP_071449.1:n.1588-3_1588-2insGGTGGA
XM_011522574.1:c.1588-3_1588-2insGGTGGA	XP_011520876.1:n.1588-3_1588-2insGGTGGA
XR_933141.1:n.466_467insTCCACC
NR_135179.1:n.438_439insTCCACC
XM_017023539.2:c.1588-3_1588-2insGGTGGA	XP_016879028.1:n.1588-3_1588-2insGGTGGA
XM_017023540.2:c.1588-3_1588-2insGGTGGA	XP_016879029.1:n.1588-3_1588-2insGGTGGA
NM_022166.4:c.1588-3_1588-2insGGTGGA MANE Select	NP_071449.1:n.1588-3_1588-2insGGTGGA