Canonical Allele Identifier: CA2434248651

Gene: VSIG4

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.66021826G= , CM000685.2:g.66021826G=	GRCh38
NC_000023.10:g.65241668G= , CM000685.1:g.65241668G=	GRCh37
NC_000023.9:g.65158393G=	NCBI36
NG_021306.1:g.23300C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374737.9:c.*437C= MANE Select	ENSP00000363869.4:n.*437C=
ENST00000651578.1:c.*887C=	ENSP00000498502.1:n.*887C=
ENST00000374737.8:c.*437C=	ENSP00000363869.4:n.*437C=
ENST00000412866.2:c.*437C=	ENSP00000394143.2:n.*437C=
ENST00000427538.5:c.1082C=
ENST00000455586.6:c.*1011C=	ENSP00000411581.2:n.*1011C=
NM_001100431.1:c.*437C=	NP_001093901.1:n.*437C=
NM_001184830.1:c.*1011C=	NP_001171759.1:n.*1011C=
NM_001184831.1:c.*1011C=	NP_001171760.1:n.*1011C=
NM_001257403.1:c.*259C=	NP_001244332.1:n.*259C=
NM_007268.2:c.*437C=	NP_009199.1:n.*437C=
XM_017029251.2:c.*259C=	XP_016884740.1:n.*259C=
NM_007268.3:c.*437C= MANE Select	NP_009199.1:n.*437C=
NM_001100431.2:c.*437C=	NP_001093901.1:n.*437C=
NM_001184831.2:c.*1011C=	NP_001171760.1:n.*1011C=
NM_001257403.2:c.*259C=	NP_001244332.1:n.*259C=
NM_001184830.2:c.*1011C=	NP_001171759.1:n.*1011C=