Canonical Allele Identifier: CA1133777811

Gene: VSIG4

Linked Data

• dbSNP Id: rs2085335489
• gnomAD v3: X-66021891-C-T
• gnomAD v4: X-66021891-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.66021891C>T , CM000685.2:g.66021891C>T	GRCh38
NC_000023.10:g.65241733C>T , CM000685.1:g.65241733C>T	GRCh37
NC_000023.9:g.65158458C>T	NCBI36
NG_021306.1:g.23235G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000374737.9:c.*372G>A MANE Select	ENSP00000363869.4:n.*372G>A
ENST00000651578.1:c.*822G>A	ENSP00000498502.1:n.*822G>A
ENST00000374737.8:c.*372G>A	ENSP00000363869.4:n.*372G>A
ENST00000412866.2:c.*372G>A	ENSP00000394143.2:n.*372G>A
ENST00000427538.5:c.1017G>A
ENST00000455586.6:c.*946G>A	ENSP00000411581.2:n.*946G>A
NM_001100431.1:c.*372G>A	NP_001093901.1:n.*372G>A
NM_001184830.1:c.*946G>A	NP_001171759.1:n.*946G>A
NM_001184831.1:c.*946G>A	NP_001171760.1:n.*946G>A
NM_001257403.1:c.*194G>A	NP_001244332.1:n.*194G>A
NM_007268.2:c.*372G>A	NP_009199.1:n.*372G>A
XM_017029251.2:c.*194G>A	XP_016884740.1:n.*194G>A
NM_007268.3:c.*372G>A MANE Select	NP_009199.1:n.*372G>A
NM_001100431.2:c.*372G>A	NP_001093901.1:n.*372G>A
NM_001184831.2:c.*946G>A	NP_001171760.1:n.*946G>A
NM_001257403.2:c.*194G>A	NP_001244332.1:n.*194G>A
NM_001184830.2:c.*946G>A	NP_001171759.1:n.*946G>A