Canonical Allele Identifier: CA2693938456

Gene: VSIG4

Linked Data

• gnomAD v4: X-66021905-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.66021907del , CM000685.2:g.66021907del	GRCh38
NC_000023.10:g.65241749del , CM000685.1:g.65241749del	GRCh37
NC_000023.9:g.65158474del	NCBI36
NG_021306.1:g.23220del

Transcript Alleles

HGVS	Amino-acid change
ENST00000374737.9:c.*357del MANE Select	ENSP00000363869.4:n.*357del
ENST00000651578.1:c.*807del	ENSP00000498502.1:n.*807del
ENST00000374737.8:c.*357del	ENSP00000363869.4:n.*357del
ENST00000412866.2:c.*357del	ENSP00000394143.2:n.*357del
ENST00000427538.5:c.1002del
ENST00000455586.6:c.*931del	ENSP00000411581.2:n.*931del
NM_001100431.1:c.*357del	NP_001093901.1:n.*357del
NM_001184830.1:c.*931del	NP_001171759.1:n.*931del
NM_001184831.1:c.*931del	NP_001171760.1:n.*931del
NM_001257403.1:c.*179del	NP_001244332.1:n.*179del
NM_007268.2:c.*357del	NP_009199.1:n.*357del
XM_017029251.2:c.*179del	XP_016884740.1:n.*179del
NM_007268.3:c.*357del MANE Select	NP_009199.1:n.*357del
NM_001100431.2:c.*357del	NP_001093901.1:n.*357del
NM_001184831.2:c.*931del	NP_001171760.1:n.*931del
NM_001257403.2:c.*179del	NP_001244332.1:n.*179del
NM_001184830.2:c.*931del	NP_001171759.1:n.*931del