Canonical Allele Identifier: CA330574837

Gene: VSIG4

Linked Data

• dbSNP Id: rs998164005
• gnomAD v3: X-66021850-G-T
• gnomAD v4: X-66021850-G-T
• MyVariant Identifiers: chrX:g.65241692G>T (hg19) ; chrX:g.66021850G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.66021850G>T , CM000685.2:g.66021850G>T	GRCh38
NC_000023.10:g.65241692G>T , CM000685.1:g.65241692G>T	GRCh37
NC_000023.9:g.65158417G>T	NCBI36
NG_021306.1:g.23276C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000374737.9:c.*413C>A MANE Select	ENSP00000363869.4:n.*413C>A
ENST00000651578.1:c.*863C>A	ENSP00000498502.1:n.*863C>A
ENST00000374737.8:c.*413C>A	ENSP00000363869.4:n.*413C>A
ENST00000412866.2:c.*413C>A	ENSP00000394143.2:n.*413C>A
ENST00000427538.5:c.1058C>A
ENST00000455586.6:c.*987C>A	ENSP00000411581.2:n.*987C>A
NM_001100431.1:c.*413C>A	NP_001093901.1:n.*413C>A
NM_001184830.1:c.*987C>A	NP_001171759.1:n.*987C>A
NM_001184831.1:c.*987C>A	NP_001171760.1:n.*987C>A
NM_001257403.1:c.*235C>A	NP_001244332.1:n.*235C>A
NM_007268.2:c.*413C>A	NP_009199.1:n.*413C>A
XM_017029251.2:c.*235C>A	XP_016884740.1:n.*235C>A
NM_007268.3:c.*413C>A MANE Select	NP_009199.1:n.*413C>A
NM_001100431.2:c.*413C>A	NP_001093901.1:n.*413C>A
NM_001184831.2:c.*987C>A	NP_001171760.1:n.*987C>A
NM_001257403.2:c.*235C>A	NP_001244332.1:n.*235C>A
NM_001184830.2:c.*987C>A	NP_001171759.1:n.*987C>A