Canonical Allele Identifier: CA718616236

Gene: XYLT1

Linked Data

• dbSNP Id: rs1382442590
• gnomAD v3: 16-17138145-G-GGGTTA
• gnomAD v4: 16-17138145-G-GGGTTA
• MyVariant Identifiers: chr16:g.17232002_17232003insGGTTA (hg19) ; chr16:g.17138145_17138146insGGTTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138146_17138150dup , CM000678.2:g.17138146_17138150dup	GRCh38
NC_000016.9:g.17232003_17232007dup , CM000678.1:g.17232003_17232007dup	GRCh37
NC_000016.8:g.17139504_17139508dup	NCBI36
NG_015843.1:g.337732_337736dup
NG_015843.2:g.337732_337736dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+205_1764+209dup MANE Select	ENSP00000261381.6:n.1764+205_1764+209dup
ENST00000261381.6:c.1764+205_1764+209dup	ENSP00000261381.6:n.1764+205_1764+209dup
NM_022166.3:c.1764+205_1764+209dup	NP_071449.1:n.1764+205_1764+209dup
XM_011522574.1:c.1764+205_1764+209dup	XP_011520876.1:n.1764+205_1764+209dup
XR_933140.1:n.336-96_336-92dup
XR_933141.1:n.175-96_175-92dup
XR_933143.1:n.237-96_237-92dup
NR_135179.1:n.147-96_147-92dup
XM_017023539.2:c.1764+205_1764+209dup	XP_016879028.1:n.1764+205_1764+209dup
XM_017023540.2:c.1764+205_1764+209dup	XP_016879029.1:n.1764+205_1764+209dup
NM_022166.4:c.1764+205_1764+209dup MANE Select	NP_071449.1:n.1764+205_1764+209dup