Canonical Allele Identifier: CA2210542873

Gene: XYLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138885_17138895delinsATCAAAGGGAT , CM000678.2:g.17138885_17138895delinsATCAAAGGGAT	GRCh38
NC_000016.9:g.17232742_17232752delinsATCAAAGGGAT , CM000678.1:g.17232742_17232752delinsATCAAAGGGAT	GRCh37
NC_000016.8:g.17140243_17140253delinsATCAAAGGGAT	NCBI36
NG_015843.1:g.336987_336997delinsATCCCTTTGAT
NG_015843.2:g.336987_336997delinsATCCCTTTGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-364_1588-354delinsATCCCTTTGAT MANE Select	ENSP00000261381.6:n.1588-364_1588-354delinsATCCCTTTGAT
ENST00000261381.6:c.1588-364_1588-354delinsATCCCTTTGAT	ENSP00000261381.6:n.1588-364_1588-354delinsATCCCTTTGAT
NM_022166.3:c.1588-364_1588-354delinsATCCCTTTGAT	NP_071449.1:n.1588-364_1588-354delinsATCCCTTTGAT
XM_011522574.1:c.1588-364_1588-354delinsATCCCTTTGAT	XP_011520876.1:n.1588-364_1588-354delinsATCCCTTTGAT
XM_017023539.2:c.1588-364_1588-354delinsATCCCTTTGAT	XP_016879028.1:n.1588-364_1588-354delinsATCCCTTTGAT
XM_017023540.2:c.1588-364_1588-354delinsATCCCTTTGAT	XP_016879029.1:n.1588-364_1588-354delinsATCCCTTTGAT
NM_022166.4:c.1588-364_1588-354delinsATCCCTTTGAT MANE Select	NP_071449.1:n.1588-364_1588-354delinsATCCCTTTGAT