Canonical Allele Identifier: CA2210541611

Gene: XYLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138231_17138235delinsATTAT , CM000678.2:g.17138231_17138235delinsATTAT	GRCh38
NC_000016.9:g.17232088_17232092delinsATTAT , CM000678.1:g.17232088_17232092delinsATTAT	GRCh37
NC_000016.8:g.17139589_17139593delinsATTAT	NCBI36
NG_015843.1:g.337647_337651delinsATAAT
NG_015843.2:g.337647_337651delinsATAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+120_1764+124delinsATAAT MANE Select	ENSP00000261381.6:n.1764+120_1764+124delinsATAAT
ENST00000261381.6:c.1764+120_1764+124delinsATAAT	ENSP00000261381.6:n.1764+120_1764+124delinsATAAT
NM_022166.3:c.1764+120_1764+124delinsATAAT	NP_071449.1:n.1764+120_1764+124delinsATAAT
XM_011522574.1:c.1764+120_1764+124delinsATAAT	XP_011520876.1:n.1764+120_1764+124delinsATAAT
XR_933140.1:n.336-11_336-7delinsATTAT
XR_933141.1:n.175-11_175-7delinsATTAT
XR_933143.1:n.237-11_237-7delinsATTAT
NR_135179.1:n.147-11_147-7delinsATTAT
XM_017023539.2:c.1764+120_1764+124delinsATAAT	XP_016879028.1:n.1764+120_1764+124delinsATAAT
XM_017023540.2:c.1764+120_1764+124delinsATAAT	XP_016879029.1:n.1764+120_1764+124delinsATAAT
NM_022166.4:c.1764+120_1764+124delinsATAAT MANE Select	NP_071449.1:n.1764+120_1764+124delinsATAAT