Canonical Allele Identifier: CA2210542442

Gene: XYLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138639_17138654delinsTTTAAAAGAATGTGGC , CM000678.2:g.17138639_17138654delinsTTTAAAAGAATGTGGC	GRCh38
NC_000016.9:g.17232496_17232511delinsTTTAAAAGAATGTGGC , CM000678.1:g.17232496_17232511delinsTTTAAAAGAATGTGGC	GRCh37
NC_000016.8:g.17139997_17140012delinsTTTAAAAGAATGTGGC	NCBI36
NG_015843.1:g.337228_337243delinsGCCACATTCTTTTAAA
NG_015843.2:g.337228_337243delinsGCCACATTCTTTTAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-123_1588-108delinsGCCACATTCTTTTAAA MANE Select	ENSP00000261381.6:n.1588-123_1588-108delinsGCCACATTCTTTTAAA
ENST00000261381.6:c.1588-123_1588-108delinsGCCACATTCTTTTAAA	ENSP00000261381.6:n.1588-123_1588-108delinsGCCACATTCTTTTAAA
NM_022166.3:c.1588-123_1588-108delinsGCCACATTCTTTTAAA	NP_071449.1:n.1588-123_1588-108delinsGCCACATTCTTTTAAA
XM_011522574.1:c.1588-123_1588-108delinsGCCACATTCTTTTAAA	XP_011520876.1:n.1588-123_1588-108delinsGCCACATTCTTTTAAA
XR_933141.1:n.572_587delinsTTTAAAAGAATGTGGC
NR_135179.1:n.544_559delinsTTTAAAAGAATGTGGC
XM_017023539.2:c.1588-123_1588-108delinsGCCACATTCTTTTAAA	XP_016879028.1:n.1588-123_1588-108delinsGCCACATTCTTTTAAA
XM_017023540.2:c.1588-123_1588-108delinsGCCACATTCTTTTAAA	XP_016879029.1:n.1588-123_1588-108delinsGCCACATTCTTTTAAA
NM_022166.4:c.1588-123_1588-108delinsGCCACATTCTTTTAAA MANE Select	NP_071449.1:n.1588-123_1588-108delinsGCCACATTCTTTTAAA