Canonical Allele Identifier: CA621656100

Gene: XYLT1

Linked Data

• dbSNP Id: rs1225784897
• gnomAD v2: 16-17232620-C-CA
• gnomAD v3: 16-17138763-C-CA
• gnomAD v4: 16-17138763-C-CA
• MyVariant Identifiers: chr16:g.17232620_17232621insA (hg19) ; chr16:g.17138763_17138764insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138768dup , CM000678.2:g.17138768dup	GRCh38
NC_000016.9:g.17232625dup , CM000678.1:g.17232625dup	GRCh37
NC_000016.8:g.17140126dup	NCBI36
NG_015843.1:g.337118dup
NG_015843.2:g.337118dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-233dup MANE Select	ENSP00000261381.6:n.1588-233dup
ENST00000261381.6:c.1588-233dup	ENSP00000261381.6:n.1588-233dup
NM_022166.3:c.1588-233dup	NP_071449.1:n.1588-233dup
XM_011522574.1:c.1588-233dup	XP_011520876.1:n.1588-233dup
XM_017023539.2:c.1588-233dup	XP_016879028.1:n.1588-233dup
XM_017023540.2:c.1588-233dup	XP_016879029.1:n.1588-233dup
NM_022166.4:c.1588-233dup MANE Select	NP_071449.1:n.1588-233dup