Canonical Allele Identifier: CA2631987573

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17138579-C-CAGATGAACTGGGGTGGGAAATGGTG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138581_17138605dup , CM000678.2:g.17138581_17138605dup	GRCh38
NC_000016.9:g.17232438_17232462dup , CM000678.1:g.17232438_17232462dup	GRCh37
NC_000016.8:g.17139939_17139963dup	NCBI36
NG_015843.1:g.337278_337302dup
NG_015843.2:g.337278_337302dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-73_1588-49dup MANE Select	ENSP00000261381.6:n.1588-73_1588-49dup
ENST00000261381.6:c.1588-73_1588-49dup	ENSP00000261381.6:n.1588-73_1588-49dup
NM_022166.3:c.1588-73_1588-49dup	NP_071449.1:n.1588-73_1588-49dup
XM_011522574.1:c.1588-73_1588-49dup	XP_011520876.1:n.1588-73_1588-49dup
XR_933141.1:n.514_538dup
NR_135179.1:n.486_510dup
XM_017023539.2:c.1588-73_1588-49dup	XP_016879028.1:n.1588-73_1588-49dup
XM_017023540.2:c.1588-73_1588-49dup	XP_016879029.1:n.1588-73_1588-49dup
NM_022166.4:c.1588-73_1588-49dup MANE Select	NP_071449.1:n.1588-73_1588-49dup