Canonical Allele Identifier: CA684178997

Gene: VSIG10

Linked Data

• dbSNP Id: rs1176481581
• MyVariant Identifiers: chr12:g.118524338C>T (hg19) ; chr12:g.118086533C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.118086533C>T , CM000674.2:g.118086533C>T	GRCh38
NC_000012.11:g.118524338C>T , CM000674.1:g.118524338C>T	GRCh37
NC_000012.10:g.117008721C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359236.10:c.362-4104G>A MANE Select	ENSP00000352172.5:n.362-4104G>A
ENST00000359236.9:c.362-4104G>A	ENSP00000352172.5:n.362-4104G>A
ENST00000536905.5:n.873-4104G>A
ENST00000538357.1:c.362-6927G>A	ENSP00000442861.1:n.362-6927G>A
NM_019086.5:c.362-4104G>A	NP_061959.2:n.362-4104G>A
XM_006719467.2:c.362-6927G>A	XP_006719530.1:n.362-6927G>A
XM_011538502.1:c.362-4104G>A	XP_011536804.1:n.362-4104G>A
XR_944592.1:n.696-4104G>A
XR_944593.1:n.696-4104G>A
XR_944594.1:n.696-4104G>A
XM_005253908.4:c.-130-4104G>A	XP_005253965.1:n.-130-4104G>A
XM_017019504.1:c.-130-4104G>A	XP_016874993.1:n.-130-4104G>A
XM_017019505.1:c.-130-4104G>A	XP_016874994.1:n.-130-4104G>A
XM_017019506.1:c.-338-4104G>A	XP_016874995.1:n.-338-4104G>A
XR_002957341.1:n.696-4104G>A
XR_002957342.1:n.696-4104G>A
XR_002957343.1:n.696-4104G>A
NM_019086.6:c.362-4104G>A MANE Select	NP_061959.2:n.362-4104G>A