Canonical Allele Identifier: CA2693938382

Gene: VSIG4

Linked Data

• gnomAD v4: X-66021819-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.66021819C>A , CM000685.2:g.66021819C>A	GRCh38
NC_000023.10:g.65241661C>A , CM000685.1:g.65241661C>A	GRCh37
NC_000023.9:g.65158386C>A	NCBI36
NG_021306.1:g.23307G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000374737.9:c.*444G>T MANE Select	ENSP00000363869.4:n.*444G>T
ENST00000651578.1:c.*894G>T	ENSP00000498502.1:n.*894G>T
ENST00000374737.8:c.*444G>T	ENSP00000363869.4:n.*444G>T
ENST00000412866.2:c.*444G>T	ENSP00000394143.2:n.*444G>T
ENST00000427538.5:c.1089G>T
ENST00000455586.6:c.*1018G>T	ENSP00000411581.2:n.*1018G>T
NM_001100431.1:c.*444G>T	NP_001093901.1:n.*444G>T
NM_001184830.1:c.*1018G>T	NP_001171759.1:n.*1018G>T
NM_001184831.1:c.*1018G>T	NP_001171760.1:n.*1018G>T
NM_001257403.1:c.*266G>T	NP_001244332.1:n.*266G>T
NM_007268.2:c.*444G>T	NP_009199.1:n.*444G>T
XM_017029251.2:c.*266G>T	XP_016884740.1:n.*266G>T
NM_007268.3:c.*444G>T MANE Select	NP_009199.1:n.*444G>T
NM_001100431.2:c.*444G>T	NP_001093901.1:n.*444G>T
NM_001184831.2:c.*1018G>T	NP_001171760.1:n.*1018G>T
NM_001257403.2:c.*266G>T	NP_001244332.1:n.*266G>T
NM_001184830.2:c.*1018G>T	NP_001171759.1:n.*1018G>T