Canonical Allele Identifier: CA919667548

Gene: XYLT1

Linked Data

• dbSNP Id: rs1597146931

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138999_17139017dup , CM000678.2:g.17138999_17139017dup	GRCh38
NC_000016.9:g.17232856_17232874dup , CM000678.1:g.17232856_17232874dup	GRCh37
NC_000016.8:g.17140357_17140375dup	NCBI36
NG_015843.1:g.336866_336884dup
NG_015843.2:g.336866_336884dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-485_1588-467dup MANE Select	ENSP00000261381.6:n.1588-485_1588-467dup
ENST00000261381.6:c.1588-485_1588-467dup	ENSP00000261381.6:n.1588-485_1588-467dup
NM_022166.3:c.1588-485_1588-467dup	NP_071449.1:n.1588-485_1588-467dup
XM_011522574.1:c.1588-485_1588-467dup	XP_011520876.1:n.1588-485_1588-467dup
XM_017023539.2:c.1588-485_1588-467dup	XP_016879028.1:n.1588-485_1588-467dup
XM_017023540.2:c.1588-485_1588-467dup	XP_016879029.1:n.1588-485_1588-467dup
NM_022166.4:c.1588-485_1588-467dup MANE Select	NP_071449.1:n.1588-485_1588-467dup