Canonical Allele Identifier: CA621656017

Gene: XYLT1

Linked Data

• dbSNP Id: rs1567291249
• gnomAD v2: 16-17232174-A-ATCACTTAGGAGGCTGGCAGACCATGAGAAAGTCTCACCTGGAAGCGGTGGAAGTCCTGCGGC
• gnomAD v3: 16-17138317-A-ATCACTTAGGAGGCTGGCAGACCATGAGAAAGTCTCACCTGGAAGCGGTGGAAGTCCTGCGGC
• gnomAD v4: 16-17138317-A-ATCACTTAGGAGGCTGGCAGACCATGAGAAAGTCTCACCTGGAAGCGGTGGAAGTCCTGCGGC
• MyVariant Identifiers: chr16:g.17232174_17232175insTCACTTAGGAGGCTGGCAGACCATGAGAAAGTCTCACCTGGAAGCGGTGGAAGTCCTGCGGC (hg19) ; chr16:g.17138317_17138318insTCACTTAGGAGGCTGGCAGACCATGAGAAAGTCTCACCTGGAAGCGGTGGAAGTCCTGCGGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138319_17138380dup , CM000678.2:g.17138319_17138380dup	GRCh38
NC_000016.9:g.17232176_17232237dup , CM000678.1:g.17232176_17232237dup	GRCh37
NC_000016.8:g.17139677_17139738dup	NCBI36
NG_015843.1:g.337503_337564dup
NG_015843.2:g.337503_337564dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1740_1764+37dup
ENST00000261381.6:c.1740_1764+37dup
NM_022166.3:c.1740_1764+37dup
XM_011522574.1:c.1740_1764+37dup
XR_933141.1:n.252_313dup
NR_135179.1:n.224_285dup
XM_017023539.2:c.1740_1764+37dup
XM_017023540.2:c.1740_1764+37dup
NM_022166.4:c.1740_1764+37dup