Canonical Allele Identifier: CA2821555409

Gene: VSIG4

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.66021895T>A , CM000685.2:g.66021895T>A	GRCh38
NC_000023.10:g.65241737T>A , CM000685.1:g.65241737T>A	GRCh37
NC_000023.9:g.65158462T>A	NCBI36
NG_021306.1:g.23231A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374737.9:c.*368A>T MANE Select	ENSP00000363869.4:n.*368A>T
ENST00000651578.1:c.*818A>T	ENSP00000498502.1:n.*818A>T
ENST00000374737.8:c.*368A>T	ENSP00000363869.4:n.*368A>T
ENST00000412866.2:c.*368A>T	ENSP00000394143.2:n.*368A>T
ENST00000427538.5:c.1013A>T
ENST00000455586.6:c.*942A>T	ENSP00000411581.2:n.*942A>T
NM_001100431.1:c.*368A>T	NP_001093901.1:n.*368A>T
NM_001184830.1:c.*942A>T	NP_001171759.1:n.*942A>T
NM_001184831.1:c.*942A>T	NP_001171760.1:n.*942A>T
NM_001257403.1:c.*190A>T	NP_001244332.1:n.*190A>T
NM_007268.2:c.*368A>T	NP_009199.1:n.*368A>T
XM_017029251.2:c.*190A>T	XP_016884740.1:n.*190A>T
NM_007268.3:c.*368A>T MANE Select	NP_009199.1:n.*368A>T
NM_001100431.2:c.*368A>T	NP_001093901.1:n.*368A>T
NM_001184831.2:c.*942A>T	NP_001171760.1:n.*942A>T
NM_001257403.2:c.*190A>T	NP_001244332.1:n.*190A>T
NM_001184830.2:c.*942A>T	NP_001171759.1:n.*942A>T