Canonical Allele Identifier: CA2210542327

Gene: XYLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138588_17138591delinsTGGG , CM000678.2:g.17138588_17138591delinsTGGG	GRCh38
NC_000016.9:g.17232445_17232448delinsTGGG , CM000678.1:g.17232445_17232448delinsTGGG	GRCh37
NC_000016.8:g.17139946_17139949delinsTGGG	NCBI36
NG_015843.1:g.337291_337294delinsCCCA
NG_015843.2:g.337291_337294delinsCCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-60_1588-57delinsCCCA MANE Select	ENSP00000261381.6:n.1588-60_1588-57delinsCCCA
ENST00000261381.6:c.1588-60_1588-57delinsCCCA	ENSP00000261381.6:n.1588-60_1588-57delinsCCCA
NM_022166.3:c.1588-60_1588-57delinsCCCA	NP_071449.1:n.1588-60_1588-57delinsCCCA
XM_011522574.1:c.1588-60_1588-57delinsCCCA	XP_011520876.1:n.1588-60_1588-57delinsCCCA
XR_933141.1:n.521_524delinsTGGG
NR_135179.1:n.493_496delinsTGGG
XM_017023539.2:c.1588-60_1588-57delinsCCCA	XP_016879028.1:n.1588-60_1588-57delinsCCCA
XM_017023540.2:c.1588-60_1588-57delinsCCCA	XP_016879029.1:n.1588-60_1588-57delinsCCCA
NM_022166.4:c.1588-60_1588-57delinsCCCA MANE Select	NP_071449.1:n.1588-60_1588-57delinsCCCA