Canonical Allele Identifier: CA2210541638

Gene: XYLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138248_17138259delinsTTGGGCACCATG , CM000678.2:g.17138248_17138259delinsTTGGGCACCATG	GRCh38
NC_000016.9:g.17232105_17232116delinsTTGGGCACCATG , CM000678.1:g.17232105_17232116delinsTTGGGCACCATG	GRCh37
NC_000016.8:g.17139606_17139617delinsTTGGGCACCATG	NCBI36
NG_015843.1:g.337623_337634delinsCATGGTGCCCAA
NG_015843.2:g.337623_337634delinsCATGGTGCCCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+96_1764+107delinsCATGGTGCCCAA MANE Select	ENSP00000261381.6:n.1764+96_1764+107delinsCATGGTGCCCAA
ENST00000261381.6:c.1764+96_1764+107delinsCATGGTGCCCAA	ENSP00000261381.6:n.1764+96_1764+107delinsCATGGTGCCCAA
NM_022166.3:c.1764+96_1764+107delinsCATGGTGCCCAA	NP_071449.1:n.1764+96_1764+107delinsCATGGTGCCCAA
XM_011522574.1:c.1764+96_1764+107delinsCATGGTGCCCAA	XP_011520876.1:n.1764+96_1764+107delinsCATGGTGCCCAA
XR_933140.1:n.342_353delinsTTGGGCACCATG
XR_933141.1:n.181_192delinsTTGGGCACCATG
XR_933143.1:n.243_254delinsTTGGGCACCATG
NR_135179.1:n.153_164delinsTTGGGCACCATG
XM_017023539.2:c.1764+96_1764+107delinsCATGGTGCCCAA	XP_016879028.1:n.1764+96_1764+107delinsCATGGTGCCCAA
XM_017023540.2:c.1764+96_1764+107delinsCATGGTGCCCAA	XP_016879029.1:n.1764+96_1764+107delinsCATGGTGCCCAA
NM_022166.4:c.1764+96_1764+107delinsCATGGTGCCCAA MANE Select	NP_071449.1:n.1764+96_1764+107delinsCATGGTGCCCAA