Canonical Allele Identifier: CA2210542139

Gene: XYLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138509_17138525delinsTCCAGGACCGTATGGAA , CM000678.2:g.17138509_17138525delinsTCCAGGACCGTATGGAA	GRCh38
NC_000016.9:g.17232366_17232382delinsTCCAGGACCGTATGGAA , CM000678.1:g.17232366_17232382delinsTCCAGGACCGTATGGAA	GRCh37
NC_000016.8:g.17139867_17139883delinsTCCAGGACCGTATGGAA	NCBI36
NG_015843.1:g.337357_337373delinsTTCCATACGGTCCTGGA
NG_015843.2:g.337357_337373delinsTTCCATACGGTCCTGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1594_1610delinsTTCCATACGGTCCTGGA MANE Select	ENSP00000261381.6:p.Phe532=
ENST00000261381.6:c.1594_1610delinsTTCCATACGGTCCTGGA	ENSP00000261381.6:p.Phe532=
NM_022166.3:c.1594_1610delinsTTCCATACGGTCCTGGA	NP_071449.1:p.Phe532=
XM_011522574.1:c.1594_1610delinsTTCCATACGGTCCTGGA	XP_011520876.1:p.Phe532=
XR_933141.1:n.442_458delinsTCCAGGACCGTATGGAA
NR_135179.1:n.414_430delinsTCCAGGACCGTATGGAA
XM_017023539.2:c.1594_1610delinsTTCCATACGGTCCTGGA	XP_016879028.1:p.Phe532=
XM_017023540.2:c.1594_1610delinsTTCCATACGGTCCTGGA	XP_016879029.1:p.Phe532=
NM_022166.4:c.1594_1610delinsTTCCATACGGTCCTGGA MANE Select	NP_071449.1:p.Phe532=