Canonical Allele Identifier: CA279080973

Gene: XYLT1

Linked Data

• dbSNP Id: rs34685043
• MyVariant Identifiers: chr16:g.17228415_17228416insA (hg19) ; chr16:g.17134558_17134559insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17134558_17134559insA , CM000678.2:g.17134558_17134559insA	GRCh38
NC_000016.9:g.17228415_17228416insA , CM000678.1:g.17228415_17228416insA	GRCh37
NC_000016.8:g.17135916_17135917insA	NCBI36
NG_015843.1:g.341323_341324insT
NG_015843.2:g.341323_341324insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1941_1942insT MANE Select	ENSP00000261381.6:p.Thr648TyrfsTer?
ENST00000261381.6:c.1941_1942insT	ENSP00000261381.6:p.Thr648TyrfsTer?
NM_022166.3:c.1941_1942insT	NP_071449.1:p.Thr648TyrfsTer?
XM_011522574.1:c.1941_1942insT	XP_011520876.1:p.Thr648TyrfsTer?
XR_933140.1:n.82+8_82+9insA
XR_933141.1:n.75+8_75+9insA
XR_933143.1:n.82+8_82+9insA
NR_135179.1:n.47+8_47+9insA
XM_017023539.2:c.1941_1942insT	XP_016879028.1:p.Thr648TyrfsTer?
XM_017023540.2:c.1941_1942insT	XP_016879029.1:p.Thr648TyrfsTer?
NM_022166.4:c.1941_1942insT MANE Select	NP_071449.1:p.Thr648TyrfsTer?