Canonical Allele Identifier: CA2210541477

Gene: XYLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138148_17138151delinsTTAA , CM000678.2:g.17138148_17138151delinsTTAA	GRCh38
NC_000016.9:g.17232005_17232008delinsTTAA , CM000678.1:g.17232005_17232008delinsTTAA	GRCh37
NC_000016.8:g.17139506_17139509delinsTTAA	NCBI36
NG_015843.1:g.337731_337734delinsTTAA
NG_015843.2:g.337731_337734delinsTTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+204_1764+207delinsTTAA MANE Select	ENSP00000261381.6:n.1764+204_1764+207delinsTTAA
ENST00000261381.6:c.1764+204_1764+207delinsTTAA	ENSP00000261381.6:n.1764+204_1764+207delinsTTAA
NM_022166.3:c.1764+204_1764+207delinsTTAA	NP_071449.1:n.1764+204_1764+207delinsTTAA
XM_011522574.1:c.1764+204_1764+207delinsTTAA	XP_011520876.1:n.1764+204_1764+207delinsTTAA
XR_933140.1:n.336-94_336-91delinsTTAA
XR_933141.1:n.175-94_175-91delinsTTAA
XR_933143.1:n.237-94_237-91delinsTTAA
NR_135179.1:n.147-94_147-91delinsTTAA
XM_017023539.2:c.1764+204_1764+207delinsTTAA	XP_016879028.1:n.1764+204_1764+207delinsTTAA
XM_017023540.2:c.1764+204_1764+207delinsTTAA	XP_016879029.1:n.1764+204_1764+207delinsTTAA
NM_022166.4:c.1764+204_1764+207delinsTTAA MANE Select	NP_071449.1:n.1764+204_1764+207delinsTTAA