Canonical Allele Identifier: CA2693938432

Gene: VSIG4

Linked Data

• gnomAD v4: X-66021878-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.66021879del , CM000685.2:g.66021879del	GRCh38
NC_000023.10:g.65241721del , CM000685.1:g.65241721del	GRCh37
NC_000023.9:g.65158446del	NCBI36
NG_021306.1:g.23247del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374737.9:c.*384del MANE Select	ENSP00000363869.4:n.*384del
ENST00000651578.1:c.*834del	ENSP00000498502.1:n.*834del
ENST00000374737.8:c.*384del	ENSP00000363869.4:n.*384del
ENST00000412866.2:c.*384del	ENSP00000394143.2:n.*384del
ENST00000427538.5:c.1029del
ENST00000455586.6:c.*958del	ENSP00000411581.2:n.*958del
NM_001100431.1:c.*384del	NP_001093901.1:n.*384del
NM_001184830.1:c.*958del	NP_001171759.1:n.*958del
NM_001184831.1:c.*958del	NP_001171760.1:n.*958del
NM_001257403.1:c.*206del	NP_001244332.1:n.*206del
NM_007268.2:c.*384del	NP_009199.1:n.*384del
XM_017029251.2:c.*206del	XP_016884740.1:n.*206del
NM_007268.3:c.*384del MANE Select	NP_009199.1:n.*384del
NM_001100431.2:c.*384del	NP_001093901.1:n.*384del
NM_001184831.2:c.*958del	NP_001171760.1:n.*958del
NM_001257403.2:c.*206del	NP_001244332.1:n.*206del
NM_001184830.2:c.*958del	NP_001171759.1:n.*958del