Canonical Allele Identifier: CA330574825

Gene: VSIG4

Linked Data

• dbSNP Id: rs1028422550
• gnomAD v3: X-66021748-G-T
• gnomAD v4: X-66021748-G-T
• MyVariant Identifiers: chrX:g.65241590G>T (hg19) ; chrX:g.66021748G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.66021748G>T , CM000685.2:g.66021748G>T	GRCh38
NC_000023.10:g.65241590G>T , CM000685.1:g.65241590G>T	GRCh37
NC_000023.9:g.65158315G>T	NCBI36
NG_021306.1:g.23378C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374737.9:c.*515C>A MANE Select	ENSP00000363869.4:n.*515C>A
ENST00000374737.8:c.*515C>A	ENSP00000363869.4:n.*515C>A
ENST00000427538.5:c.1160C>A
ENST00000455586.6:c.*1089C>A	ENSP00000411581.2:n.*1089C>A
NM_001100431.1:c.*515C>A	NP_001093901.1:n.*515C>A
NM_001184830.1:c.*1089C>A	NP_001171759.1:n.*1089C>A
NM_001184831.1:c.*1089C>A	NP_001171760.1:n.*1089C>A
NM_001257403.1:c.*337C>A	NP_001244332.1:n.*337C>A
NM_007268.2:c.*515C>A	NP_009199.1:n.*515C>A
XM_017029251.2:c.*337C>A	XP_016884740.1:n.*337C>A
NM_007268.3:c.*515C>A MANE Select	NP_009199.1:n.*515C>A
NM_001100431.2:c.*515C>A	NP_001093901.1:n.*515C>A
NM_001184831.2:c.*1089C>A	NP_001171760.1:n.*1089C>A
NM_001257403.2:c.*337C>A	NP_001244332.1:n.*337C>A
NM_001184830.2:c.*1089C>A	NP_001171759.1:n.*1089C>A