Canonical Allele Identifier: CA621654979

Gene: XYLT1

Linked Data

• dbSNP Id: rs1555481569
• gnomAD v2: 16-17232025-G-GAACATCCCTGAAGTAAGTGCT
• gnomAD v3: 16-17138168-G-GAACATCCCTGAAGTAAGTGCT
• gnomAD v4: 16-17138168-G-GAACATCCCTGAAGTAAGTGCT
• MyVariant Identifiers: chr16:g.17232025_17232026insAACATCCCTGAAGTAAGTGCT (hg19) ; chr16:g.17138168_17138169insAACATCCCTGAAGTAAGTGCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138169_17138189dup , CM000678.2:g.17138169_17138189dup	GRCh38
NC_000016.9:g.17232026_17232046dup , CM000678.1:g.17232026_17232046dup	GRCh37
NC_000016.8:g.17139527_17139547dup	NCBI36
NG_015843.1:g.337693_337713dup
NG_015843.2:g.337693_337713dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+166_1764+186dup MANE Select	ENSP00000261381.6:n.1764+166_1764+186dup
ENST00000261381.6:c.1764+166_1764+186dup	ENSP00000261381.6:n.1764+166_1764+186dup
NM_022166.3:c.1764+166_1764+186dup	NP_071449.1:n.1764+166_1764+186dup
XM_011522574.1:c.1764+166_1764+186dup	XP_011520876.1:n.1764+166_1764+186dup
XR_933140.1:n.336-73_336-53dup
XR_933141.1:n.175-73_175-53dup
XR_933143.1:n.237-73_237-53dup
NR_135179.1:n.147-73_147-53dup
XM_017023539.2:c.1764+166_1764+186dup	XP_016879028.1:n.1764+166_1764+186dup
XM_017023540.2:c.1764+166_1764+186dup	XP_016879029.1:n.1764+166_1764+186dup
NM_022166.4:c.1764+166_1764+186dup MANE Select	NP_071449.1:n.1764+166_1764+186dup