Canonical Allele Identifier: CA621656094

Gene: XYLT1

Linked Data

• dbSNP Id: rs1469786024
• gnomAD v2: 16-17232377-A-ATGGAAGAAGGACTGCAGGGGAGAGAGGGACCCAGCCTGAGACCTCT
• gnomAD v4: 16-17138520-A-ATGGAAGAAGGACTGCAGGGGAGAGAGGGACCCAGCCTGAGACCTCT
• MyVariant Identifiers: chr16:g.17232377_17232378insTGGAAGAAGGACTGCAGGGGAGAGAGGGACCCAGCCTGAGACCTCT (hg19) ; chr16:g.17138520_17138521insTGGAAGAAGGACTGCAGGGGAGAGAGGGACCCAGCCTGAGACCTCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138521_17138566dup , CM000678.2:g.17138521_17138566dup	GRCh38
NC_000016.9:g.17232378_17232423dup , CM000678.1:g.17232378_17232423dup	GRCh37
NC_000016.8:g.17139879_17139924dup	NCBI36
NG_015843.1:g.337316_337361dup
NG_015843.2:g.337316_337361dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000261381.7:c.1588-35_1598dup
ENST00000261381.6:c.1588-35_1598dup
NM_022166.3:c.1588-35_1598dup
XM_011522574.1:c.1588-35_1598dup
XR_933141.1:n.454_499dup
NR_135179.1:n.426_471dup
XM_017023539.2:c.1588-35_1598dup
XM_017023540.2:c.1588-35_1598dup
NM_022166.4:c.1588-35_1598dup