Canonical Allele Identifier: CA642301703
Gene: VSIG4 HGNC NCBI

Linked Data

dbSNP Id: rs1364187704

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.66021762del , CM000685.2:g.66021762del GRCh38
NC_000023.10:g.65241604del , CM000685.1:g.65241604del GRCh37
NC_000023.9:g.65158329del NCBI36
NG_021306.1:g.23365del

Transcript Alleles

HGVS Amino-acid Change
ENST00000374737.9:c.*502del MANE Select ENSP00000363869.4:n.*502del
ENST00000374737.8:c.*502del ENSP00000363869.4:n.*502del
ENST00000427538.5:c.1147del
ENST00000455586.6:c.*1076del ENSP00000411581.2:n.*1076del
NM_001100431.1:c.*502del NP_001093901.1:n.*502del
NM_001184830.1:c.*1076del NP_001171759.1:n.*1076del
NM_001184831.1:c.*1076del NP_001171760.1:n.*1076del
NM_001257403.1:c.*324del NP_001244332.1:n.*324del
NM_007268.2:c.*502del NP_009199.1:n.*502del
XM_017029251.2:c.*324del XP_016884740.1:n.*324del
NM_007268.3:c.*502del MANE Select NP_009199.1:n.*502del
NM_001100431.2:c.*502del NP_001093901.1:n.*502del
NM_001184831.2:c.*1076del NP_001171760.1:n.*1076del
NM_001257403.2:c.*324del NP_001244332.1:n.*324del
NM_001184830.2:c.*1076del NP_001171759.1:n.*1076del