Canonical Allele Identifier: CA493797206

Gene: XYLT1

Linked Data

• MyVariant Identifiers: chr16:g.17232008_17232009insTGAG (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138153_17138156dup , CM000678.2:g.17138153_17138156dup	GRCh38
NC_000016.9:g.17232010_17232013dup , CM000678.1:g.17232010_17232013dup	GRCh37
NC_000016.8:g.17139511_17139514dup	NCBI36
NG_015843.1:g.337727_337730dup
NG_015843.2:g.337727_337730dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+200_1764+203dup MANE Select	ENSP00000261381.6:n.1764+200_1764+203dup
ENST00000261381.6:c.1764+200_1764+203dup	ENSP00000261381.6:n.1764+200_1764+203dup
NM_022166.3:c.1764+200_1764+203dup	NP_071449.1:n.1764+200_1764+203dup
XM_011522574.1:c.1764+200_1764+203dup	XP_011520876.1:n.1764+200_1764+203dup
XR_933140.1:n.336-89_336-86dup
XR_933141.1:n.175-89_175-86dup
XR_933143.1:n.237-89_237-86dup
NR_135179.1:n.147-89_147-86dup
XM_017023539.2:c.1764+200_1764+203dup	XP_016879028.1:n.1764+200_1764+203dup
XM_017023540.2:c.1764+200_1764+203dup	XP_016879029.1:n.1764+200_1764+203dup
NM_022166.4:c.1764+200_1764+203dup MANE Select	NP_071449.1:n.1764+200_1764+203dup