Canonical Allele Identifier: CA2210542203

Gene: XYLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138545_17138546delinsAG , CM000678.2:g.17138545_17138546delinsAG	GRCh38
NC_000016.9:g.17232402_17232403delinsAG , CM000678.1:g.17232402_17232403delinsAG	GRCh37
NC_000016.8:g.17139903_17139904delinsAG	NCBI36
NG_015843.1:g.337336_337337delinsCT
NG_015843.2:g.337336_337337delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-15_1588-14delinsCT MANE Select	ENSP00000261381.6:n.1588-15_1588-14delinsCT
ENST00000261381.6:c.1588-15_1588-14delinsCT	ENSP00000261381.6:n.1588-15_1588-14delinsCT
NM_022166.3:c.1588-15_1588-14delinsCT	NP_071449.1:n.1588-15_1588-14delinsCT
XM_011522574.1:c.1588-15_1588-14delinsCT	XP_011520876.1:n.1588-15_1588-14delinsCT
XR_933141.1:n.478_479delinsAG
NR_135179.1:n.450_451delinsAG
XM_017023539.2:c.1588-15_1588-14delinsCT	XP_016879028.1:n.1588-15_1588-14delinsCT
XM_017023540.2:c.1588-15_1588-14delinsCT	XP_016879029.1:n.1588-15_1588-14delinsCT
NM_022166.4:c.1588-15_1588-14delinsCT MANE Select	NP_071449.1:n.1588-15_1588-14delinsCT