Canonical Allele Identifier: CA2210542217

Gene: XYLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138549_17138566delinsACCCAGCCTGAGACCTCT , CM000678.2:g.17138549_17138566delinsACCCAGCCTGAGACCTCT	GRCh38
NC_000016.9:g.17232406_17232423delinsACCCAGCCTGAGACCTCT , CM000678.1:g.17232406_17232423delinsACCCAGCCTGAGACCTCT	GRCh37
NC_000016.8:g.17139907_17139924delinsACCCAGCCTGAGACCTCT	NCBI36
NG_015843.1:g.337316_337333delinsAGAGGTCTCAGGCTGGGT
NG_015843.2:g.337316_337333delinsAGAGGTCTCAGGCTGGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-35_1588-18delinsAGAGGTCTCAGGCTGGGT MANE Select	ENSP00000261381.6:n.1588-35_1588-18delinsAGAGGTCTCAGGCTGGGT
ENST00000261381.6:c.1588-35_1588-18delinsAGAGGTCTCAGGCTGGGT	ENSP00000261381.6:n.1588-35_1588-18delinsAGAGGTCTCAGGCTGGGT
NM_022166.3:c.1588-35_1588-18delinsAGAGGTCTCAGGCTGGGT	NP_071449.1:n.1588-35_1588-18delinsAGAGGTCTCAGGCTGGGT
XM_011522574.1:c.1588-35_1588-18delinsAGAGGTCTCAGGCTGGGT	XP_011520876.1:n.1588-35_1588-18delinsAGAGGTCTCAGGCTGGGT
XR_933141.1:n.482_499delinsACCCAGCCTGAGACCTCT
NR_135179.1:n.454_471delinsACCCAGCCTGAGACCTCT
XM_017023539.2:c.1588-35_1588-18delinsAGAGGTCTCAGGCTGGGT	XP_016879028.1:n.1588-35_1588-18delinsAGAGGTCTCAGGCTGGGT
XM_017023540.2:c.1588-35_1588-18delinsAGAGGTCTCAGGCTGGGT	XP_016879029.1:n.1588-35_1588-18delinsAGAGGTCTCAGGCTGGGT
NM_022166.4:c.1588-35_1588-18delinsAGAGGTCTCAGGCTGGGT MANE Select	NP_071449.1:n.1588-35_1588-18delinsAGAGGTCTCAGGCTGGGT