Canonical Allele Identifier: CA2575925878

Gene: XYLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138333_17138342del , CM000678.2:g.17138333_17138342del	GRCh38
NC_000016.9:g.17232190_17232199del , CM000678.1:g.17232190_17232199del	GRCh37
NC_000016.8:g.17139691_17139700del	NCBI36
NG_015843.1:g.337542_337551del
NG_015843.2:g.337542_337551del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+15_1764+24del MANE Select	ENSP00000261381.6:n.1764+15_1764+24del
ENST00000261381.6:c.1764+15_1764+24del	ENSP00000261381.6:n.1764+15_1764+24del
NM_022166.3:c.1764+15_1764+24del	NP_071449.1:n.1764+15_1764+24del
XM_011522574.1:c.1764+15_1764+24del	XP_011520876.1:n.1764+15_1764+24del
XR_933140.1:n.427_436del
XR_933141.1:n.266_275del
XR_933143.1:n.328_337del
NR_135179.1:n.238_247del
XM_017023539.2:c.1764+15_1764+24del	XP_016879028.1:n.1764+15_1764+24del
XM_017023540.2:c.1764+15_1764+24del	XP_016879029.1:n.1764+15_1764+24del
NM_022166.4:c.1764+15_1764+24del MANE Select	NP_071449.1:n.1764+15_1764+24del