Canonical Allele Identifier: CA2210543004

Gene: XYLT1

Linked Data

• dbSNP Id: rs2030877064

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138999_17139019dup , CM000678.2:g.17138999_17139019dup	GRCh38
NC_000016.9:g.17232856_17232876dup , CM000678.1:g.17232856_17232876dup	GRCh37
NC_000016.8:g.17140357_17140377dup	NCBI36
NG_015843.1:g.336865_336885dup
NG_015843.2:g.336865_336885dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-486_1588-466dup MANE Select	ENSP00000261381.6:n.1588-486_1588-466dup
ENST00000261381.6:c.1588-486_1588-466dup	ENSP00000261381.6:n.1588-486_1588-466dup
NM_022166.3:c.1588-486_1588-466dup	NP_071449.1:n.1588-486_1588-466dup
XM_011522574.1:c.1588-486_1588-466dup	XP_011520876.1:n.1588-486_1588-466dup
XM_017023539.2:c.1588-486_1588-466dup	XP_016879028.1:n.1588-486_1588-466dup
XM_017023540.2:c.1588-486_1588-466dup	XP_016879029.1:n.1588-486_1588-466dup
NM_022166.4:c.1588-486_1588-466dup MANE Select	NP_071449.1:n.1588-486_1588-466dup