Canonical Allele Identifier: CA2525879827

Gene: VSIG4

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.66021885A>G , CM000685.2:g.66021885A>G	GRCh38
NC_000023.10:g.65241727A>G , CM000685.1:g.65241727A>G	GRCh37
NC_000023.9:g.65158452A>G	NCBI36
NG_021306.1:g.23241T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000374737.9:c.*378T>C MANE Select	ENSP00000363869.4:n.*378T>C
ENST00000651578.1:c.*828T>C	ENSP00000498502.1:n.*828T>C
ENST00000374737.8:c.*378T>C	ENSP00000363869.4:n.*378T>C
ENST00000412866.2:c.*378T>C	ENSP00000394143.2:n.*378T>C
ENST00000427538.5:c.1023T>C
ENST00000455586.6:c.*952T>C	ENSP00000411581.2:n.*952T>C
NM_001100431.1:c.*378T>C	NP_001093901.1:n.*378T>C
NM_001184830.1:c.*952T>C	NP_001171759.1:n.*952T>C
NM_001184831.1:c.*952T>C	NP_001171760.1:n.*952T>C
NM_001257403.1:c.*200T>C	NP_001244332.1:n.*200T>C
NM_007268.2:c.*378T>C	NP_009199.1:n.*378T>C
XM_017029251.2:c.*200T>C	XP_016884740.1:n.*200T>C
NM_007268.3:c.*378T>C MANE Select	NP_009199.1:n.*378T>C
NM_001100431.2:c.*378T>C	NP_001093901.1:n.*378T>C
NM_001184831.2:c.*952T>C	NP_001171760.1:n.*952T>C
NM_001257403.2:c.*200T>C	NP_001244332.1:n.*200T>C
NM_001184830.2:c.*952T>C	NP_001171759.1:n.*952T>C