Canonical Allele Identifier: CA718616463

Gene: XYLT1

Linked Data

• dbSNP Id: rs1330787580
• gnomAD v3: 16-17138323-T-TAGGAGGCTGGCAGACCATG
• gnomAD v4: 16-17138323-T-TAGGAGGCTGGCAGACCATG
• MyVariant Identifiers: chr16:g.17232180_17232181insAGGAGGCTGGCAGACCATG (hg19) ; chr16:g.17138323_17138324insAGGAGGCTGGCAGACCATG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138326_17138344dup , CM000678.2:g.17138326_17138344dup	GRCh38
NC_000016.9:g.17232183_17232201dup , CM000678.1:g.17232183_17232201dup	GRCh37
NC_000016.8:g.17139684_17139702dup	NCBI36
NG_015843.1:g.337540_337558dup
NG_015843.2:g.337540_337558dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+13_1764+31dup MANE Select	ENSP00000261381.6:n.1764+13_1764+31dup
ENST00000261381.6:c.1764+13_1764+31dup	ENSP00000261381.6:n.1764+13_1764+31dup
NM_022166.3:c.1764+13_1764+31dup	NP_071449.1:n.1764+13_1764+31dup
XM_011522574.1:c.1764+13_1764+31dup	XP_011520876.1:n.1764+13_1764+31dup
XR_933140.1:n.420_438dup
XR_933141.1:n.259_277dup
XR_933143.1:n.321_339dup
NR_135179.1:n.231_249dup
XM_017023539.2:c.1764+13_1764+31dup	XP_016879028.1:n.1764+13_1764+31dup
XM_017023540.2:c.1764+13_1764+31dup	XP_016879029.1:n.1764+13_1764+31dup
NM_022166.4:c.1764+13_1764+31dup MANE Select	NP_071449.1:n.1764+13_1764+31dup