Canonical Allele Identifier: CA2210538677

Gene: XYLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17134440_17134452delinsAGCTCTCCTCTCT , CM000678.2:g.17134440_17134452delinsAGCTCTCCTCTCT	GRCh38
NC_000016.9:g.17228297_17228309delinsAGCTCTCCTCTCT , CM000678.1:g.17228297_17228309delinsAGCTCTCCTCTCT	GRCh37
NC_000016.8:g.17135798_17135810delinsAGCTCTCCTCTCT	NCBI36
NG_015843.1:g.341430_341442delinsAGAGAGGAGAGCT
NG_015843.2:g.341430_341442delinsAGAGAGGAGAGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.2027+21_2027+33delinsAGAGAGGAGAGCT MANE Select	ENSP00000261381.6:n.2027+21_2027+33delinsAGAGAGGAGAGCT
ENST00000261381.6:c.2027+21_2027+33delinsAGAGAGGAGAGCT	ENSP00000261381.6:n.2027+21_2027+33delinsAGAGAGGAGAGCT
NM_022166.3:c.2027+21_2027+33delinsAGAGAGGAGAGCT	NP_071449.1:n.2027+21_2027+33delinsAGAGAGGAGAGCT
XM_011522574.1:c.2027+21_2027+33delinsAGAGAGGAGAGCT	XP_011520876.1:n.2027+21_2027+33delinsAGAGAGGAGAGCT
XM_017023539.2:c.2027+21_2027+33delinsAGAGAGGAGAGCT	XP_016879028.1:n.2027+21_2027+33delinsAGAGAGGAGAGCT
XM_017023540.2:c.2027+21_2027+33delinsAGAGAGGAGAGCT	XP_016879029.1:n.2027+21_2027+33delinsAGAGAGGAGAGCT
NM_022166.4:c.2027+21_2027+33delinsAGAGAGGAGAGCT MANE Select	NP_071449.1:n.2027+21_2027+33delinsAGAGAGGAGAGCT