Canonical Allele Identifier: CA2631987539

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17138321-CTTAGGAGGCTGGCAGACCATGA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138322_17138343del , CM000678.2:g.17138322_17138343del	GRCh38
NC_000016.9:g.17232179_17232200del , CM000678.1:g.17232179_17232200del	GRCh37
NC_000016.8:g.17139680_17139701del	NCBI36
NG_015843.1:g.337539_337560del
NG_015843.2:g.337539_337560del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+12_1764+33del MANE Select	ENSP00000261381.6:n.1764+12_1764+33del
ENST00000261381.6:c.1764+12_1764+33del	ENSP00000261381.6:n.1764+12_1764+33del
NM_022166.3:c.1764+12_1764+33del	NP_071449.1:n.1764+12_1764+33del
XM_011522574.1:c.1764+12_1764+33del	XP_011520876.1:n.1764+12_1764+33del
XR_933140.1:n.416_437del
XR_933141.1:n.255_276del
XR_933143.1:n.317_338del
NR_135179.1:n.227_248del
XM_017023539.2:c.1764+12_1764+33del	XP_016879028.1:n.1764+12_1764+33del
XM_017023540.2:c.1764+12_1764+33del	XP_016879029.1:n.1764+12_1764+33del
NM_022166.4:c.1764+12_1764+33del MANE Select	NP_071449.1:n.1764+12_1764+33del