Canonical Allele Identifier: CA2631987506

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17138253-C-CACCATGTGATAAGATG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138257_17138272dup , CM000678.2:g.17138257_17138272dup	GRCh38
NC_000016.9:g.17232114_17232129dup , CM000678.1:g.17232114_17232129dup	GRCh37
NC_000016.8:g.17139615_17139630dup	NCBI36
NG_015843.1:g.337613_337628dup
NG_015843.2:g.337613_337628dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+86_1764+101dup MANE Select	ENSP00000261381.6:n.1764+86_1764+101dup
ENST00000261381.6:c.1764+86_1764+101dup	ENSP00000261381.6:n.1764+86_1764+101dup
NM_022166.3:c.1764+86_1764+101dup	NP_071449.1:n.1764+86_1764+101dup
XM_011522574.1:c.1764+86_1764+101dup	XP_011520876.1:n.1764+86_1764+101dup
XR_933140.1:n.351_366dup
XR_933141.1:n.190_205dup
XR_933143.1:n.252_267dup
NR_135179.1:n.162_177dup
XM_017023539.2:c.1764+86_1764+101dup	XP_016879028.1:n.1764+86_1764+101dup
XM_017023540.2:c.1764+86_1764+101dup	XP_016879029.1:n.1764+86_1764+101dup
NM_022166.4:c.1764+86_1764+101dup MANE Select	NP_071449.1:n.1764+86_1764+101dup