Canonical Allele Identifier: CA2434248633

Gene: VSIG4

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.66021786A= , CM000685.2:g.66021786A=	GRCh38
NC_000023.10:g.65241628A= , CM000685.1:g.65241628A=	GRCh37
NC_000023.9:g.65158353A=	NCBI36
NG_021306.1:g.23340T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374737.9:c.*477T= MANE Select	ENSP00000363869.4:n.*477T=
ENST00000651578.1:c.*927T=	ENSP00000498502.1:n.*927T=
ENST00000374737.8:c.*477T=	ENSP00000363869.4:n.*477T=
ENST00000412866.2:c.*477T=	ENSP00000394143.2:n.*477T=
ENST00000427538.5:c.1122T=
ENST00000455586.6:c.*1051T=	ENSP00000411581.2:n.*1051T=
NM_001100431.1:c.*477T=	NP_001093901.1:n.*477T=
NM_001184830.1:c.*1051T=	NP_001171759.1:n.*1051T=
NM_001184831.1:c.*1051T=	NP_001171760.1:n.*1051T=
NM_001257403.1:c.*299T=	NP_001244332.1:n.*299T=
NM_007268.2:c.*477T=	NP_009199.1:n.*477T=
XM_017029251.2:c.*299T=	XP_016884740.1:n.*299T=
NM_007268.3:c.*477T= MANE Select	NP_009199.1:n.*477T=
NM_001100431.2:c.*477T=	NP_001093901.1:n.*477T=
NM_001184831.2:c.*1051T=	NP_001171760.1:n.*1051T=
NM_001257403.2:c.*299T=	NP_001244332.1:n.*299T=
NM_001184830.2:c.*1051T=	NP_001171759.1:n.*1051T=