Canonical Allele Identifier: CA2693938337

Gene: VSIG4

Linked Data

• gnomAD v4: X-66021738-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.66021738T>A , CM000685.2:g.66021738T>A	GRCh38
NC_000023.10:g.65241580T>A , CM000685.1:g.65241580T>A	GRCh37
NC_000023.9:g.65158305T>A	NCBI36
NG_021306.1:g.23388A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374737.9:c.*525A>T MANE Select	ENSP00000363869.4:n.*525A>T
ENST00000374737.8:c.*525A>T	ENSP00000363869.4:n.*525A>T
ENST00000427538.5:c.1170A>T
NM_001100431.1:c.*525A>T	NP_001093901.1:n.*525A>T
NM_001184830.1:c.*1099A>T	NP_001171759.1:n.*1099A>T
NM_001184831.1:c.*1099A>T	NP_001171760.1:n.*1099A>T
NM_001257403.1:c.*347A>T	NP_001244332.1:n.*347A>T
NM_007268.2:c.*525A>T	NP_009199.1:n.*525A>T
XM_017029251.2:c.*347A>T	XP_016884740.1:n.*347A>T
NM_007268.3:c.*525A>T MANE Select	NP_009199.1:n.*525A>T
NM_001100431.2:c.*525A>T	NP_001093901.1:n.*525A>T
NM_001184831.2:c.*1099A>T	NP_001171760.1:n.*1099A>T
NM_001257403.2:c.*347A>T	NP_001244332.1:n.*347A>T
NM_001184830.2:c.*1099A>T	NP_001171759.1:n.*1099A>T