Canonical Allele Identifier: CA2552570978

Gene: XYLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138724_17138728dup , CM000678.2:g.17138724_17138728dup	GRCh38
NC_000016.9:g.17232581_17232585dup , CM000678.1:g.17232581_17232585dup	GRCh37
NC_000016.8:g.17140082_17140086dup	NCBI36
NG_015843.1:g.337154_337158dup
NG_015843.2:g.337154_337158dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-197_1588-193dup MANE Select	ENSP00000261381.6:n.1588-197_1588-193dup
ENST00000261381.6:c.1588-197_1588-193dup	ENSP00000261381.6:n.1588-197_1588-193dup
NM_022166.3:c.1588-197_1588-193dup	NP_071449.1:n.1588-197_1588-193dup
XM_011522574.1:c.1588-197_1588-193dup	XP_011520876.1:n.1588-197_1588-193dup
XR_933141.1:n.657_661dup
NR_135179.1:n.629_633dup
XM_017023539.2:c.1588-197_1588-193dup	XP_016879028.1:n.1588-197_1588-193dup
XM_017023540.2:c.1588-197_1588-193dup	XP_016879029.1:n.1588-197_1588-193dup
NM_022166.4:c.1588-197_1588-193dup MANE Select	NP_071449.1:n.1588-197_1588-193dup