Canonical Allele Identifier: CA2210541631

Gene: XYLT1

Linked Data

• dbSNP Id: rs2030830947

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138238_17138247del , CM000678.2:g.17138238_17138247del	GRCh38
NC_000016.9:g.17232095_17232104del , CM000678.1:g.17232095_17232104del	GRCh37
NC_000016.8:g.17139596_17139605del	NCBI36
NG_015843.1:g.337635_337644del
NG_015843.2:g.337635_337644del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+108_1764+117del MANE Select	ENSP00000261381.6:n.1764+108_1764+117del
ENST00000261381.6:c.1764+108_1764+117del	ENSP00000261381.6:n.1764+108_1764+117del
NM_022166.3:c.1764+108_1764+117del	NP_071449.1:n.1764+108_1764+117del
XM_011522574.1:c.1764+108_1764+117del	XP_011520876.1:n.1764+108_1764+117del
XR_933140.1:n.336-4_341del
XR_933141.1:n.175-4_180del
XR_933143.1:n.237-4_242del
NR_135179.1:n.147-4_152del
XM_017023539.2:c.1764+108_1764+117del	XP_016879028.1:n.1764+108_1764+117del
XM_017023540.2:c.1764+108_1764+117del	XP_016879029.1:n.1764+108_1764+117del
NM_022166.4:c.1764+108_1764+117del MANE Select	NP_071449.1:n.1764+108_1764+117del