Canonical Allele Identifier: CA2210542332

Gene: XYLT1

Linked Data

• dbSNP Id: rs2030856600

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138590_17138592del , CM000678.2:g.17138590_17138592del	GRCh38
NC_000016.9:g.17232447_17232449del , CM000678.1:g.17232447_17232449del	GRCh37
NC_000016.8:g.17139948_17139950del	NCBI36
NG_015843.1:g.337291_337293del
NG_015843.2:g.337291_337293del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-60_1588-58del MANE Select	ENSP00000261381.6:n.1588-60_1588-58del
ENST00000261381.6:c.1588-60_1588-58del	ENSP00000261381.6:n.1588-60_1588-58del
NM_022166.3:c.1588-60_1588-58del	NP_071449.1:n.1588-60_1588-58del
XM_011522574.1:c.1588-60_1588-58del	XP_011520876.1:n.1588-60_1588-58del
XR_933141.1:n.523_525del
NR_135179.1:n.495_497del
XM_017023539.2:c.1588-60_1588-58del	XP_016879028.1:n.1588-60_1588-58del
XM_017023540.2:c.1588-60_1588-58del	XP_016879029.1:n.1588-60_1588-58del
NM_022166.4:c.1588-60_1588-58del MANE Select	NP_071449.1:n.1588-60_1588-58del