Canonical Allele Identifier: CA2210541439

Gene: XYLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138118_17138128delinsAATAATGAAAG , CM000678.2:g.17138118_17138128delinsAATAATGAAAG	GRCh38
NC_000016.9:g.17231975_17231985delinsAATAATGAAAG , CM000678.1:g.17231975_17231985delinsAATAATGAAAG	GRCh37
NC_000016.8:g.17139476_17139486delinsAATAATGAAAG	NCBI36
NG_015843.1:g.337754_337764delinsCTTTCATTATT
NG_015843.2:g.337754_337764delinsCTTTCATTATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+227_1764+237delinsCTTTCATTATT MANE Select	ENSP00000261381.6:n.1764+227_1764+237delinsCTTTCATTATT
ENST00000261381.6:c.1764+227_1764+237delinsCTTTCATTATT	ENSP00000261381.6:n.1764+227_1764+237delinsCTTTCATTATT
NM_022166.3:c.1764+227_1764+237delinsCTTTCATTATT	NP_071449.1:n.1764+227_1764+237delinsCTTTCATTATT
XM_011522574.1:c.1764+227_1764+237delinsCTTTCATTATT	XP_011520876.1:n.1764+227_1764+237delinsCTTTCATTATT
XR_933140.1:n.336-124_336-114delinsAATAATGAAAG
XR_933141.1:n.175-124_175-114delinsAATAATGAAAG
XR_933143.1:n.237-124_237-114delinsAATAATGAAAG
NR_135179.1:n.147-124_147-114delinsAATAATGAAAG
XM_017023539.2:c.1764+227_1764+237delinsCTTTCATTATT	XP_016879028.1:n.1764+227_1764+237delinsCTTTCATTATT
XM_017023540.2:c.1764+227_1764+237delinsCTTTCATTATT	XP_016879029.1:n.1764+227_1764+237delinsCTTTCATTATT
NM_022166.4:c.1764+227_1764+237delinsCTTTCATTATT MANE Select	NP_071449.1:n.1764+227_1764+237delinsCTTTCATTATT