Canonical Allele Identifier: CA718616207

Gene: XYLT1

Linked Data

• dbSNP Id: rs1470924047
• gnomAD v3: 16-17138094-G-GTTTTCATATCCCTAAAATGGAATAA
• gnomAD v4: 16-17138094-G-GTTTTCATATCCCTAAAATGGAATAA
• MyVariant Identifiers: chr16:g.17231951_17231952insTTTTCATATCCCTAAAATGGAATAA (hg19) ; chr16:g.17138094_17138095insTTTTCATATCCCTAAAATGGAATAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138096_17138120dup , CM000678.2:g.17138096_17138120dup	GRCh38
NC_000016.9:g.17231953_17231977dup , CM000678.1:g.17231953_17231977dup	GRCh37
NC_000016.8:g.17139454_17139478dup	NCBI36
NG_015843.1:g.337763_337787dup
NG_015843.2:g.337763_337787dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+236_1764+260dup MANE Select	ENSP00000261381.6:n.1764+236_1764+260dup
ENST00000261381.6:c.1764+236_1764+260dup	ENSP00000261381.6:n.1764+236_1764+260dup
NM_022166.3:c.1764+236_1764+260dup	NP_071449.1:n.1764+236_1764+260dup
XM_011522574.1:c.1764+236_1764+260dup	XP_011520876.1:n.1764+236_1764+260dup
XR_933140.1:n.336-146_336-122dup
XR_933141.1:n.175-146_175-122dup
XR_933143.1:n.237-146_237-122dup
NR_135179.1:n.147-146_147-122dup
XM_017023539.2:c.1764+236_1764+260dup	XP_016879028.1:n.1764+236_1764+260dup
XM_017023540.2:c.1764+236_1764+260dup	XP_016879029.1:n.1764+236_1764+260dup
NM_022166.4:c.1764+236_1764+260dup MANE Select	NP_071449.1:n.1764+236_1764+260dup