Canonical Allele Identifier: CA2631987389

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17138189-TCAATAAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138192_17138198del , CM000678.2:g.17138192_17138198del	GRCh38
NC_000016.9:g.17232049_17232055del , CM000678.1:g.17232049_17232055del	GRCh37
NC_000016.8:g.17139550_17139556del	NCBI36
NG_015843.1:g.337686_337692del
NG_015843.2:g.337686_337692del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+159_1764+165del MANE Select	ENSP00000261381.6:n.1764+159_1764+165del
ENST00000261381.6:c.1764+159_1764+165del	ENSP00000261381.6:n.1764+159_1764+165del
NM_022166.3:c.1764+159_1764+165del	NP_071449.1:n.1764+159_1764+165del
XM_011522574.1:c.1764+159_1764+165del	XP_011520876.1:n.1764+159_1764+165del
XR_933140.1:n.336-50_336-44del
XR_933141.1:n.175-50_175-44del
XR_933143.1:n.237-50_237-44del
NR_135179.1:n.147-50_147-44del
XM_017023539.2:c.1764+159_1764+165del	XP_016879028.1:n.1764+159_1764+165del
XM_017023540.2:c.1764+159_1764+165del	XP_016879029.1:n.1764+159_1764+165del
NM_022166.4:c.1764+159_1764+165del MANE Select	NP_071449.1:n.1764+159_1764+165del