Canonical Allele Identifier: CA684179021

Gene: VSIG10

Linked Data

• dbSNP Id: rs1212316990
• MyVariant Identifiers: chr12:g.118524380A>G (hg19) ; chr12:g.118086575A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.118086575A>G , CM000674.2:g.118086575A>G	GRCh38
NC_000012.11:g.118524380A>G , CM000674.1:g.118524380A>G	GRCh37
NC_000012.10:g.117008763A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359236.10:c.362-4146T>C MANE Select	ENSP00000352172.5:n.362-4146T>C
ENST00000359236.9:c.362-4146T>C	ENSP00000352172.5:n.362-4146T>C
ENST00000536905.5:n.873-4146T>C
ENST00000538357.1:c.362-6969T>C	ENSP00000442861.1:n.362-6969T>C
NM_019086.5:c.362-4146T>C	NP_061959.2:n.362-4146T>C
XM_006719467.2:c.362-6969T>C	XP_006719530.1:n.362-6969T>C
XM_011538502.1:c.362-4146T>C	XP_011536804.1:n.362-4146T>C
XR_944592.1:n.696-4146T>C
XR_944593.1:n.696-4146T>C
XR_944594.1:n.696-4146T>C
XM_005253908.4:c.-130-4146T>C	XP_005253965.1:n.-130-4146T>C
XM_017019504.1:c.-130-4146T>C	XP_016874993.1:n.-130-4146T>C
XM_017019505.1:c.-130-4146T>C	XP_016874994.1:n.-130-4146T>C
XM_017019506.1:c.-338-4146T>C	XP_016874995.1:n.-338-4146T>C
XR_002957341.1:n.696-4146T>C
XR_002957342.1:n.696-4146T>C
XR_002957343.1:n.696-4146T>C
NM_019086.6:c.362-4146T>C MANE Select	NP_061959.2:n.362-4146T>C