Canonical Allele Identifier: CA2631987566

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17138558-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138558_17138559insT , CM000678.2:g.17138558_17138559insT	GRCh38
NC_000016.9:g.17232415_17232416insT , CM000678.1:g.17232415_17232416insT	GRCh37
NC_000016.8:g.17139916_17139917insT	NCBI36
NG_015843.1:g.337323_337324insA
NG_015843.2:g.337323_337324insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-28_1588-27insA MANE Select	ENSP00000261381.6:n.1588-28_1588-27insA
ENST00000261381.6:c.1588-28_1588-27insA	ENSP00000261381.6:n.1588-28_1588-27insA
NM_022166.3:c.1588-28_1588-27insA	NP_071449.1:n.1588-28_1588-27insA
XM_011522574.1:c.1588-28_1588-27insA	XP_011520876.1:n.1588-28_1588-27insA
XR_933141.1:n.491_492insT
NR_135179.1:n.463_464insT
XM_017023539.2:c.1588-28_1588-27insA	XP_016879028.1:n.1588-28_1588-27insA
XM_017023540.2:c.1588-28_1588-27insA	XP_016879029.1:n.1588-28_1588-27insA
NM_022166.4:c.1588-28_1588-27insA MANE Select	NP_071449.1:n.1588-28_1588-27insA