Canonical Allele Identifier: CA2210538856

Gene: XYLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17134780_17134787delinsCTGGGGGT , CM000678.2:g.17134780_17134787delinsCTGGGGGT	GRCh38
NC_000016.9:g.17228637_17228644delinsCTGGGGGT , CM000678.1:g.17228637_17228644delinsCTGGGGGT	GRCh37
NC_000016.8:g.17136138_17136145delinsCTGGGGGT	NCBI36
NG_015843.1:g.341095_341102delinsACCCCCAG
NG_015843.2:g.341095_341102delinsACCCCCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1765-52_1765-45delinsACCCCCAG MANE Select	ENSP00000261381.6:n.1765-52_1765-45delinsACCCCCAG
ENST00000261381.6:c.1765-52_1765-45delinsACCCCCAG	ENSP00000261381.6:n.1765-52_1765-45delinsACCCCCAG
NM_022166.3:c.1765-52_1765-45delinsACCCCCAG	NP_071449.1:n.1765-52_1765-45delinsACCCCCAG
XM_011522574.1:c.1765-52_1765-45delinsACCCCCAG	XP_011520876.1:n.1765-52_1765-45delinsACCCCCAG
XR_933140.1:n.82+230_82+237delinsCTGGGGGT
XR_933141.1:n.75+230_75+237delinsCTGGGGGT
XR_933143.1:n.82+230_82+237delinsCTGGGGGT
NR_135179.1:n.47+230_47+237delinsCTGGGGGT
XM_017023539.2:c.1765-52_1765-45delinsACCCCCAG	XP_016879028.1:n.1765-52_1765-45delinsACCCCCAG
XM_017023540.2:c.1765-52_1765-45delinsACCCCCAG	XP_016879029.1:n.1765-52_1765-45delinsACCCCCAG
NM_022166.4:c.1765-52_1765-45delinsACCCCCAG MANE Select	NP_071449.1:n.1765-52_1765-45delinsACCCCCAG