Canonical Allele Identifier: CA2434248705

Gene: VSIG4

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.66021947C= , CM000685.2:g.66021947C=	GRCh38
NC_000023.10:g.65241789C= , CM000685.1:g.65241789C=	GRCh37
NC_000023.9:g.65158514C=	NCBI36
NG_021306.1:g.23179G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374737.9:c.*316G= MANE Select	ENSP00000363869.4:n.*316G=
ENST00000651578.1:c.*766G=	ENSP00000498502.1:n.*766G=
ENST00000374737.8:c.*316G=	ENSP00000363869.4:n.*316G=
ENST00000412866.2:c.*316G=	ENSP00000394143.2:n.*316G=
ENST00000427538.5:c.961G=
ENST00000455586.6:c.*890G=	ENSP00000411581.2:n.*890G=
NM_001100431.1:c.*316G=	NP_001093901.1:n.*316G=
NM_001184830.1:c.*890G=	NP_001171759.1:n.*890G=
NM_001184831.1:c.*890G=	NP_001171760.1:n.*890G=
NM_001257403.1:c.*138G=	NP_001244332.1:n.*138G=
NM_007268.2:c.*316G=	NP_009199.1:n.*316G=
XM_017029251.2:c.*138G=	XP_016884740.1:n.*138G=
NM_007268.3:c.*316G= MANE Select	NP_009199.1:n.*316G=
NM_001100431.2:c.*316G=	NP_001093901.1:n.*316G=
NM_001184831.2:c.*890G=	NP_001171760.1:n.*890G=
NM_001257403.2:c.*138G=	NP_001244332.1:n.*138G=
NM_001184830.2:c.*890G=	NP_001171759.1:n.*890G=