Canonical Allele Identifier: CA642301706

Gene: VSIG4

Linked Data

• dbSNP Id: rs1212499205
• gnomAD v2: X-65241606-A-G
• gnomAD v4: X-66021764-A-G
• MyVariant Identifiers: chrX:g.65241606A>G (hg19) ; chrX:g.66021764A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.66021764A>G , CM000685.2:g.66021764A>G	GRCh38
NC_000023.10:g.65241606A>G , CM000685.1:g.65241606A>G	GRCh37
NC_000023.9:g.65158331A>G	NCBI36
NG_021306.1:g.23362T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374737.9:c.*499T>C MANE Select	ENSP00000363869.4:n.*499T>C
ENST00000374737.8:c.*499T>C	ENSP00000363869.4:n.*499T>C
ENST00000427538.5:c.1144T>C
ENST00000455586.6:c.*1073T>C	ENSP00000411581.2:n.*1073T>C
NM_001100431.1:c.*499T>C	NP_001093901.1:n.*499T>C
NM_001184830.1:c.*1073T>C	NP_001171759.1:n.*1073T>C
NM_001184831.1:c.*1073T>C	NP_001171760.1:n.*1073T>C
NM_001257403.1:c.*321T>C	NP_001244332.1:n.*321T>C
NM_007268.2:c.*499T>C	NP_009199.1:n.*499T>C
XM_017029251.2:c.*321T>C	XP_016884740.1:n.*321T>C
NM_007268.3:c.*499T>C MANE Select	NP_009199.1:n.*499T>C
NM_001100431.2:c.*499T>C	NP_001093901.1:n.*499T>C
NM_001184831.2:c.*1073T>C	NP_001171760.1:n.*1073T>C
NM_001257403.2:c.*321T>C	NP_001244332.1:n.*321T>C
NM_001184830.2:c.*1073T>C	NP_001171759.1:n.*1073T>C