Canonical Allele Identifier: CA2434248740

Gene: VSIG4

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.66022023G= , CM000685.2:g.66022023G=	GRCh38
NC_000023.10:g.65241865G= , CM000685.1:g.65241865G=	GRCh37
NC_000023.9:g.65158590G=	NCBI36
NG_021306.1:g.23103C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374737.9:c.*240C= MANE Select	ENSP00000363869.4:n.*240C=
ENST00000651578.1:c.*690C=	ENSP00000498502.1:n.*690C=
ENST00000374737.8:c.*240C=	ENSP00000363869.4:n.*240C=
ENST00000412866.2:c.*240C=	ENSP00000394143.2:n.*240C=
ENST00000427538.5:c.885C=
ENST00000455586.6:c.*814C=	ENSP00000411581.2:n.*814C=
NM_001100431.1:c.*240C=	NP_001093901.1:n.*240C=
NM_001184830.1:c.*814C=	NP_001171759.1:n.*814C=
NM_001184831.1:c.*814C=	NP_001171760.1:n.*814C=
NM_001257403.1:c.*62C=	NP_001244332.1:n.*62C=
NM_007268.2:c.*240C=	NP_009199.1:n.*240C=
XM_017029251.2:c.*62C=	XP_016884740.1:n.*62C=
NM_007268.3:c.*240C= MANE Select	NP_009199.1:n.*240C=
NM_001100431.2:c.*240C=	NP_001093901.1:n.*240C=
NM_001184831.2:c.*814C=	NP_001171760.1:n.*814C=
NM_001257403.2:c.*62C=	NP_001244332.1:n.*62C=
NM_001184830.2:c.*814C=	NP_001171759.1:n.*814C=