Canonical Allele Identifier: CA877388483

Gene: VSIG4

Linked Data

• dbSNP Id: rs1482391264
• gnomAD v4: X-66021900-T-C
• MyVariant Identifiers: chrX:g.65241742T>C (hg19) ; chrX:g.66021900T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.66021900T>C , CM000685.2:g.66021900T>C	GRCh38
NC_000023.10:g.65241742T>C , CM000685.1:g.65241742T>C	GRCh37
NC_000023.9:g.65158467T>C	NCBI36
NG_021306.1:g.23226A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000374737.9:c.*363A>G MANE Select	ENSP00000363869.4:n.*363A>G
ENST00000651578.1:c.*813A>G	ENSP00000498502.1:n.*813A>G
ENST00000374737.8:c.*363A>G	ENSP00000363869.4:n.*363A>G
ENST00000412866.2:c.*363A>G	ENSP00000394143.2:n.*363A>G
ENST00000427538.5:c.1008A>G
ENST00000455586.6:c.*937A>G	ENSP00000411581.2:n.*937A>G
NM_001100431.1:c.*363A>G	NP_001093901.1:n.*363A>G
NM_001184830.1:c.*937A>G	NP_001171759.1:n.*937A>G
NM_001184831.1:c.*937A>G	NP_001171760.1:n.*937A>G
NM_001257403.1:c.*185A>G	NP_001244332.1:n.*185A>G
NM_007268.2:c.*363A>G	NP_009199.1:n.*363A>G
XM_017029251.2:c.*185A>G	XP_016884740.1:n.*185A>G
NM_007268.3:c.*363A>G MANE Select	NP_009199.1:n.*363A>G
NM_001100431.2:c.*363A>G	NP_001093901.1:n.*363A>G
NM_001184831.2:c.*937A>G	NP_001171760.1:n.*937A>G
NM_001257403.2:c.*185A>G	NP_001244332.1:n.*185A>G
NM_001184830.2:c.*937A>G	NP_001171759.1:n.*937A>G