Canonical Allele Identifier: CA2210538925

Gene: XYLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17134907_17134920delinsATAAGGGTGTGAGT , CM000678.2:g.17134907_17134920delinsATAAGGGTGTGAGT	GRCh38
NC_000016.9:g.17228764_17228777delinsATAAGGGTGTGAGT , CM000678.1:g.17228764_17228777delinsATAAGGGTGTGAGT	GRCh37
NC_000016.8:g.17136265_17136278delinsATAAGGGTGTGAGT	NCBI36
NG_015843.1:g.340962_340975delinsACTCACACCCTTAT
NG_015843.2:g.340962_340975delinsACTCACACCCTTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1765-185_1765-172delinsACTCACACCCTTAT MANE Select	ENSP00000261381.6:n.1765-185_1765-172delinsACTCACACCCTTAT
ENST00000261381.6:c.1765-185_1765-172delinsACTCACACCCTTAT	ENSP00000261381.6:n.1765-185_1765-172delinsACTCACACCCTTAT
NM_022166.3:c.1765-185_1765-172delinsACTCACACCCTTAT	NP_071449.1:n.1765-185_1765-172delinsACTCACACCCTTAT
XM_011522574.1:c.1765-185_1765-172delinsACTCACACCCTTAT	XP_011520876.1:n.1765-185_1765-172delinsACTCACACCCTTAT
XR_933140.1:n.82+357_82+370delinsATAAGGGTGTGAGT
XR_933141.1:n.75+357_75+370delinsATAAGGGTGTGAGT
XR_933143.1:n.82+357_82+370delinsATAAGGGTGTGAGT
NR_135179.1:n.47+357_47+370delinsATAAGGGTGTGAGT
XM_017023539.2:c.1765-185_1765-172delinsACTCACACCCTTAT	XP_016879028.1:n.1765-185_1765-172delinsACTCACACCCTTAT
XM_017023540.2:c.1765-185_1765-172delinsACTCACACCCTTAT	XP_016879029.1:n.1765-185_1765-172delinsACTCACACCCTTAT
NM_022166.4:c.1765-185_1765-172delinsACTCACACCCTTAT MANE Select	NP_071449.1:n.1765-185_1765-172delinsACTCACACCCTTAT