Canonical Allele Identifier: CA2693938387

Gene: VSIG4

Linked Data

• gnomAD v4: X-66021827-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.66021827T>A , CM000685.2:g.66021827T>A	GRCh38
NC_000023.10:g.65241669T>A , CM000685.1:g.65241669T>A	GRCh37
NC_000023.9:g.65158394T>A	NCBI36
NG_021306.1:g.23299A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374737.9:c.*436A>T MANE Select	ENSP00000363869.4:n.*436A>T
ENST00000651578.1:c.*886A>T	ENSP00000498502.1:n.*886A>T
ENST00000374737.8:c.*436A>T	ENSP00000363869.4:n.*436A>T
ENST00000412866.2:c.*436A>T	ENSP00000394143.2:n.*436A>T
ENST00000427538.5:c.1081A>T
ENST00000455586.6:c.*1010A>T	ENSP00000411581.2:n.*1010A>T
NM_001100431.1:c.*436A>T	NP_001093901.1:n.*436A>T
NM_001184830.1:c.*1010A>T	NP_001171759.1:n.*1010A>T
NM_001184831.1:c.*1010A>T	NP_001171760.1:n.*1010A>T
NM_001257403.1:c.*258A>T	NP_001244332.1:n.*258A>T
NM_007268.2:c.*436A>T	NP_009199.1:n.*436A>T
XM_017029251.2:c.*258A>T	XP_016884740.1:n.*258A>T
NM_007268.3:c.*436A>T MANE Select	NP_009199.1:n.*436A>T
NM_001100431.2:c.*436A>T	NP_001093901.1:n.*436A>T
NM_001184831.2:c.*1010A>T	NP_001171760.1:n.*1010A>T
NM_001257403.2:c.*258A>T	NP_001244332.1:n.*258A>T
NM_001184830.2:c.*1010A>T	NP_001171759.1:n.*1010A>T