Canonical Allele Identifier: CA621654973

Gene: XYLT1

Linked Data

• dbSNP Id: rs1475028469
• gnomAD v2: 16-17231965-A-AAAATGGAATAATAAT
• gnomAD v3: 16-17138108-A-AAAATGGAATAATAAT
• gnomAD v4: 16-17138108-A-AAAATGGAATAATAAT
• MyVariant Identifiers: chr16:g.17231965_17231966insAAATGGAATAATAAT (hg19) ; chr16:g.17138108_17138109insAAATGGAATAATAAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138109_17138123dup , CM000678.2:g.17138109_17138123dup	GRCh38
NC_000016.9:g.17231966_17231980dup , CM000678.1:g.17231966_17231980dup	GRCh37
NC_000016.8:g.17139467_17139481dup	NCBI36
NG_015843.1:g.337759_337773dup
NG_015843.2:g.337759_337773dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+232_1764+246dup MANE Select	ENSP00000261381.6:n.1764+232_1764+246dup
ENST00000261381.6:c.1764+232_1764+246dup	ENSP00000261381.6:n.1764+232_1764+246dup
NM_022166.3:c.1764+232_1764+246dup	NP_071449.1:n.1764+232_1764+246dup
XM_011522574.1:c.1764+232_1764+246dup	XP_011520876.1:n.1764+232_1764+246dup
XR_933140.1:n.336-133_336-119dup
XR_933141.1:n.175-133_175-119dup
XR_933143.1:n.237-133_237-119dup
NR_135179.1:n.147-133_147-119dup
XM_017023539.2:c.1764+232_1764+246dup	XP_016879028.1:n.1764+232_1764+246dup
XM_017023540.2:c.1764+232_1764+246dup	XP_016879029.1:n.1764+232_1764+246dup
NM_022166.4:c.1764+232_1764+246dup MANE Select	NP_071449.1:n.1764+232_1764+246dup