Canonical Allele Identifier: CA2066353265

Gene: VSIG10

Linked Data

• dbSNP Id: rs2033136006

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.118086620dup , CM000674.2:g.118086620dup	GRCh38
NC_000012.11:g.118524425dup , CM000674.1:g.118524425dup	GRCh37
NC_000012.10:g.117008808dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359236.10:c.362-4191dup MANE Select	ENSP00000352172.5:n.362-4191dup
ENST00000359236.9:c.362-4191dup	ENSP00000352172.5:n.362-4191dup
ENST00000536905.5:n.873-4191dup
ENST00000538357.1:c.362-7014dup	ENSP00000442861.1:n.362-7014dup
NM_019086.5:c.362-4191dup	NP_061959.2:n.362-4191dup
XM_006719467.2:c.362-7014dup	XP_006719530.1:n.362-7014dup
XM_011538502.1:c.362-4191dup	XP_011536804.1:n.362-4191dup
XR_944592.1:n.696-4191dup
XR_944593.1:n.696-4191dup
XR_944594.1:n.696-4191dup
XM_005253908.4:c.-130-4191dup	XP_005253965.1:n.-130-4191dup
XM_017019504.1:c.-130-4191dup	XP_016874993.1:n.-130-4191dup
XM_017019505.1:c.-130-4191dup	XP_016874994.1:n.-130-4191dup
XM_017019506.1:c.-338-4191dup	XP_016874995.1:n.-338-4191dup
XR_002957341.1:n.696-4191dup
XR_002957342.1:n.696-4191dup
XR_002957343.1:n.696-4191dup
NM_019086.6:c.362-4191dup MANE Select	NP_061959.2:n.362-4191dup