Canonical Allele Identifier: CA2434248626

Gene: VSIG4

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.66021760_66021761delinsAT , CM000685.2:g.66021760_66021761delinsAT	GRCh38
NC_000023.10:g.65241602_65241603delinsAT , CM000685.1:g.65241602_65241603delinsAT	GRCh37
NC_000023.9:g.65158327_65158328delinsAT	NCBI36
NG_021306.1:g.23365_23366delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000374737.9:c.*502_*503delinsAT MANE Select	ENSP00000363869.4:n.*502_*503delinsAT
ENST00000374737.8:c.*502_*503delinsAT	ENSP00000363869.4:n.*502_*503delinsAT
ENST00000427538.5:c.1147_1148delinsAT
ENST00000455586.6:c.*1076_*1077delinsAT	ENSP00000411581.2:n.*1076_*1077delinsAT
NM_001100431.1:c.*502_*503delinsAT	NP_001093901.1:n.*502_*503delinsAT
NM_001184830.1:c.*1076_*1077delinsAT	NP_001171759.1:n.*1076_*1077delinsAT
NM_001184831.1:c.*1076_*1077delinsAT	NP_001171760.1:n.*1076_*1077delinsAT
NM_001257403.1:c.*324_*325delinsAT	NP_001244332.1:n.*324_*325delinsAT
NM_007268.2:c.*502_*503delinsAT	NP_009199.1:n.*502_*503delinsAT
XM_017029251.2:c.*324_*325delinsAT	XP_016884740.1:n.*324_*325delinsAT
NM_007268.3:c.*502_*503delinsAT MANE Select	NP_009199.1:n.*502_*503delinsAT
NM_001100431.2:c.*502_*503delinsAT	NP_001093901.1:n.*502_*503delinsAT
NM_001184831.2:c.*1076_*1077delinsAT	NP_001171760.1:n.*1076_*1077delinsAT
NM_001257403.2:c.*324_*325delinsAT	NP_001244332.1:n.*324_*325delinsAT
NM_001184830.2:c.*1076_*1077delinsAT	NP_001171759.1:n.*1076_*1077delinsAT