Canonical Allele Identifier: CA2631987581

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17138599-A-ATGGTGAACCCT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138602_17138612dup , CM000678.2:g.17138602_17138612dup	GRCh38
NC_000016.9:g.17232459_17232469dup , CM000678.1:g.17232459_17232469dup	GRCh37
NC_000016.8:g.17139960_17139970dup	NCBI36
NG_015843.1:g.337272_337282dup
NG_015843.2:g.337272_337282dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-79_1588-69dup MANE Select	ENSP00000261381.6:n.1588-79_1588-69dup
ENST00000261381.6:c.1588-79_1588-69dup	ENSP00000261381.6:n.1588-79_1588-69dup
NM_022166.3:c.1588-79_1588-69dup	NP_071449.1:n.1588-79_1588-69dup
XM_011522574.1:c.1588-79_1588-69dup	XP_011520876.1:n.1588-79_1588-69dup
XR_933141.1:n.535_545dup
NR_135179.1:n.507_517dup
XM_017023539.2:c.1588-79_1588-69dup	XP_016879028.1:n.1588-79_1588-69dup
XM_017023540.2:c.1588-79_1588-69dup	XP_016879029.1:n.1588-79_1588-69dup
NM_022166.4:c.1588-79_1588-69dup MANE Select	NP_071449.1:n.1588-79_1588-69dup