Canonical Allele Identifier: CA2631987632

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17138741-C-CAGATTTTCCTTCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138744_17138757dup , CM000678.2:g.17138744_17138757dup	GRCh38
NC_000016.9:g.17232601_17232614dup , CM000678.1:g.17232601_17232614dup	GRCh37
NC_000016.8:g.17140102_17140115dup	NCBI36
NG_015843.1:g.337127_337140dup
NG_015843.2:g.337127_337140dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-224_1588-211dup MANE Select	ENSP00000261381.6:n.1588-224_1588-211dup
ENST00000261381.6:c.1588-224_1588-211dup	ENSP00000261381.6:n.1588-224_1588-211dup
NM_022166.3:c.1588-224_1588-211dup	NP_071449.1:n.1588-224_1588-211dup
XM_011522574.1:c.1588-224_1588-211dup	XP_011520876.1:n.1588-224_1588-211dup
XM_017023539.2:c.1588-224_1588-211dup	XP_016879028.1:n.1588-224_1588-211dup
XM_017023540.2:c.1588-224_1588-211dup	XP_016879029.1:n.1588-224_1588-211dup
NM_022166.4:c.1588-224_1588-211dup MANE Select	NP_071449.1:n.1588-224_1588-211dup