Canonical Allele Identifier: CA718616290

Gene: XYLT1

Linked Data

• dbSNP Id: rs1341108656
• MyVariant Identifiers: chr16:g.17232041_17232042insGAACATCCCTGAAGTGC (hg19) ; chr16:g.17138184_17138185insGAACATCCCTGAAGTGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138185_17138186insAACATCCCTGAAGTGCG , CM000678.2:g.17138185_17138186insAACATCCCTGAAGTGCG	GRCh38
NC_000016.9:g.17232042_17232043insAACATCCCTGAAGTGCG , CM000678.1:g.17232042_17232043insAACATCCCTGAAGTGCG	GRCh37
NC_000016.8:g.17139543_17139544insAACATCCCTGAAGTGCG	NCBI36
NG_015843.1:g.337697_337698insGCACTTCAGGGATGTTC
NG_015843.2:g.337697_337698insGCACTTCAGGGATGTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+170_1764+171insGCACTTCAGGGATGTTC MANE Select	ENSP00000261381.6:n.1764+170_1764+171insGCACTTCAGGGATGTTC
ENST00000261381.6:c.1764+170_1764+171insGCACTTCAGGGATGTTC	ENSP00000261381.6:n.1764+170_1764+171insGCACTTCAGGGATGTTC
NM_022166.3:c.1764+170_1764+171insGCACTTCAGGGATGTTC	NP_071449.1:n.1764+170_1764+171insGCACTTCAGGGATGTTC
XM_011522574.1:c.1764+170_1764+171insGCACTTCAGGGATGTTC	XP_011520876.1:n.1764+170_1764+171insGCACTTCAGGGATGTTC
XR_933140.1:n.336-57_336-56insAACATCCCTGAAGTGCG
XR_933141.1:n.175-57_175-56insAACATCCCTGAAGTGCG
XR_933143.1:n.237-57_237-56insAACATCCCTGAAGTGCG
NR_135179.1:n.147-57_147-56insAACATCCCTGAAGTGCG
XM_017023539.2:c.1764+170_1764+171insGCACTTCAGGGATGTTC	XP_016879028.1:n.1764+170_1764+171insGCACTTCAGGGATGTTC
XM_017023540.2:c.1764+170_1764+171insGCACTTCAGGGATGTTC	XP_016879029.1:n.1764+170_1764+171insGCACTTCAGGGATGTTC
NM_022166.4:c.1764+170_1764+171insGCACTTCAGGGATGTTC MANE Select	NP_071449.1:n.1764+170_1764+171insGCACTTCAGGGATGTTC