Canonical Allele Identifier: CA2210542999

Gene: XYLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138996_17139010delinsCGGCAACATAGGGAA , CM000678.2:g.17138996_17139010delinsCGGCAACATAGGGAA	GRCh38
NC_000016.9:g.17232853_17232867delinsCGGCAACATAGGGAA , CM000678.1:g.17232853_17232867delinsCGGCAACATAGGGAA	GRCh37
NC_000016.8:g.17140354_17140368delinsCGGCAACATAGGGAA	NCBI36
NG_015843.1:g.336872_336886delinsTTCCCTATGTTGCCG
NG_015843.2:g.336872_336886delinsTTCCCTATGTTGCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-479_1588-465delinsTTCCCTATGTTGCCG MANE Select	ENSP00000261381.6:n.1588-479_1588-465delinsTTCCCTATGTTGCCG
ENST00000261381.6:c.1588-479_1588-465delinsTTCCCTATGTTGCCG	ENSP00000261381.6:n.1588-479_1588-465delinsTTCCCTATGTTGCCG
NM_022166.3:c.1588-479_1588-465delinsTTCCCTATGTTGCCG	NP_071449.1:n.1588-479_1588-465delinsTTCCCTATGTTGCCG
XM_011522574.1:c.1588-479_1588-465delinsTTCCCTATGTTGCCG	XP_011520876.1:n.1588-479_1588-465delinsTTCCCTATGTTGCCG
XM_017023539.2:c.1588-479_1588-465delinsTTCCCTATGTTGCCG	XP_016879028.1:n.1588-479_1588-465delinsTTCCCTATGTTGCCG
XM_017023540.2:c.1588-479_1588-465delinsTTCCCTATGTTGCCG	XP_016879029.1:n.1588-479_1588-465delinsTTCCCTATGTTGCCG
NM_022166.4:c.1588-479_1588-465delinsTTCCCTATGTTGCCG MANE Select	NP_071449.1:n.1588-479_1588-465delinsTTCCCTATGTTGCCG