Canonical Allele Identifier: CA621656109

Gene: XYLT1

Linked Data

• dbSNP Id: rs1567291787
• gnomAD v2: 16-17232783-A-AATT
• gnomAD v3: 16-17138926-A-AATT
• gnomAD v4: 16-17138926-A-AATT
• MyVariant Identifiers: chr16:g.17232783_17232784insATT (hg19) ; chr16:g.17138926_17138927insATT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138927_17138929dup , CM000678.2:g.17138927_17138929dup	GRCh38
NC_000016.9:g.17232784_17232786dup , CM000678.1:g.17232784_17232786dup	GRCh37
NC_000016.8:g.17140285_17140287dup	NCBI36
NG_015843.1:g.336953_336955dup
NG_015843.2:g.336953_336955dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-398_1588-396dup MANE Select	ENSP00000261381.6:n.1588-398_1588-396dup
ENST00000261381.6:c.1588-398_1588-396dup	ENSP00000261381.6:n.1588-398_1588-396dup
NM_022166.3:c.1588-398_1588-396dup	NP_071449.1:n.1588-398_1588-396dup
XM_011522574.1:c.1588-398_1588-396dup	XP_011520876.1:n.1588-398_1588-396dup
XM_017023539.2:c.1588-398_1588-396dup	XP_016879028.1:n.1588-398_1588-396dup
XM_017023540.2:c.1588-398_1588-396dup	XP_016879029.1:n.1588-398_1588-396dup
NM_022166.4:c.1588-398_1588-396dup MANE Select	NP_071449.1:n.1588-398_1588-396dup