Canonical Allele Identifier: CA2210541582

Gene: XYLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138224_17138228delinsATTAT , CM000678.2:g.17138224_17138228delinsATTAT	GRCh38
NC_000016.9:g.17232081_17232085delinsATTAT , CM000678.1:g.17232081_17232085delinsATTAT	GRCh37
NC_000016.8:g.17139582_17139586delinsATTAT	NCBI36
NG_015843.1:g.337654_337658delinsATAAT
NG_015843.2:g.337654_337658delinsATAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+127_1764+131delinsATAAT MANE Select	ENSP00000261381.6:n.1764+127_1764+131delinsATAAT
ENST00000261381.6:c.1764+127_1764+131delinsATAAT	ENSP00000261381.6:n.1764+127_1764+131delinsATAAT
NM_022166.3:c.1764+127_1764+131delinsATAAT	NP_071449.1:n.1764+127_1764+131delinsATAAT
XM_011522574.1:c.1764+127_1764+131delinsATAAT	XP_011520876.1:n.1764+127_1764+131delinsATAAT
XR_933140.1:n.336-18_336-14delinsATTAT
XR_933141.1:n.175-18_175-14delinsATTAT
XR_933143.1:n.237-18_237-14delinsATTAT
NR_135179.1:n.147-18_147-14delinsATTAT
XM_017023539.2:c.1764+127_1764+131delinsATAAT	XP_016879028.1:n.1764+127_1764+131delinsATAAT
XM_017023540.2:c.1764+127_1764+131delinsATAAT	XP_016879029.1:n.1764+127_1764+131delinsATAAT
NM_022166.4:c.1764+127_1764+131delinsATAAT MANE Select	NP_071449.1:n.1764+127_1764+131delinsATAAT