Canonical Allele Identifier: CA2806078126

Gene: XYLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138773_17138783dup , CM000678.2:g.17138773_17138783dup	GRCh38
NC_000016.9:g.17232630_17232640dup , CM000678.1:g.17232630_17232640dup	GRCh37
NC_000016.8:g.17140131_17140141dup	NCBI36
NG_015843.1:g.337101_337111dup
NG_015843.2:g.337101_337111dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-250_1588-240dup MANE Select	ENSP00000261381.6:n.1588-250_1588-240dup
ENST00000261381.6:c.1588-250_1588-240dup	ENSP00000261381.6:n.1588-250_1588-240dup
NM_022166.3:c.1588-250_1588-240dup	NP_071449.1:n.1588-250_1588-240dup
XM_011522574.1:c.1588-250_1588-240dup	XP_011520876.1:n.1588-250_1588-240dup
XM_017023539.2:c.1588-250_1588-240dup	XP_016879028.1:n.1588-250_1588-240dup
XM_017023540.2:c.1588-250_1588-240dup	XP_016879029.1:n.1588-250_1588-240dup
NM_022166.4:c.1588-250_1588-240dup MANE Select	NP_071449.1:n.1588-250_1588-240dup