Canonical Allele Identifier: CA2434248660

Gene: VSIG4

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.66021850G= , CM000685.2:g.66021850G=	GRCh38
NC_000023.10:g.65241692G= , CM000685.1:g.65241692G=	GRCh37
NC_000023.9:g.65158417G=	NCBI36
NG_021306.1:g.23276C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000374737.9:c.*413C= MANE Select	ENSP00000363869.4:n.*413C=
ENST00000651578.1:c.*863C=	ENSP00000498502.1:n.*863C=
ENST00000374737.8:c.*413C=	ENSP00000363869.4:n.*413C=
ENST00000412866.2:c.*413C=	ENSP00000394143.2:n.*413C=
ENST00000427538.5:c.1058C=
ENST00000455586.6:c.*987C=	ENSP00000411581.2:n.*987C=
NM_001100431.1:c.*413C=	NP_001093901.1:n.*413C=
NM_001184830.1:c.*987C=	NP_001171759.1:n.*987C=
NM_001184831.1:c.*987C=	NP_001171760.1:n.*987C=
NM_001257403.1:c.*235C=	NP_001244332.1:n.*235C=
NM_007268.2:c.*413C=	NP_009199.1:n.*413C=
XM_017029251.2:c.*235C=	XP_016884740.1:n.*235C=
NM_007268.3:c.*413C= MANE Select	NP_009199.1:n.*413C=
NM_001100431.2:c.*413C=	NP_001093901.1:n.*413C=
NM_001184831.2:c.*987C=	NP_001171760.1:n.*987C=
NM_001257403.2:c.*235C=	NP_001244332.1:n.*235C=
NM_001184830.2:c.*987C=	NP_001171759.1:n.*987C=