Canonical Allele Identifier: CA330574849

Gene: VSIG4

Linked Data

• dbSNP Id: rs913341731
• gnomAD v4: X-66021928-G-T
• MyVariant Identifiers: chrX:g.65241770G>T (hg19) ; chrX:g.66021928G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.66021928G>T , CM000685.2:g.66021928G>T	GRCh38
NC_000023.10:g.65241770G>T , CM000685.1:g.65241770G>T	GRCh37
NC_000023.9:g.65158495G>T	NCBI36
NG_021306.1:g.23198C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000374737.9:c.*335C>A MANE Select	ENSP00000363869.4:n.*335C>A
ENST00000651578.1:c.*785C>A	ENSP00000498502.1:n.*785C>A
ENST00000374737.8:c.*335C>A	ENSP00000363869.4:n.*335C>A
ENST00000412866.2:c.*335C>A	ENSP00000394143.2:n.*335C>A
ENST00000427538.5:c.980C>A
ENST00000455586.6:c.*909C>A	ENSP00000411581.2:n.*909C>A
NM_001100431.1:c.*335C>A	NP_001093901.1:n.*335C>A
NM_001184830.1:c.*909C>A	NP_001171759.1:n.*909C>A
NM_001184831.1:c.*909C>A	NP_001171760.1:n.*909C>A
NM_001257403.1:c.*157C>A	NP_001244332.1:n.*157C>A
NM_007268.2:c.*335C>A	NP_009199.1:n.*335C>A
XM_017029251.2:c.*157C>A	XP_016884740.1:n.*157C>A
NM_007268.3:c.*335C>A MANE Select	NP_009199.1:n.*335C>A
NM_001100431.2:c.*335C>A	NP_001093901.1:n.*335C>A
NM_001184831.2:c.*909C>A	NP_001171760.1:n.*909C>A
NM_001257403.2:c.*157C>A	NP_001244332.1:n.*157C>A
NM_001184830.2:c.*909C>A	NP_001171759.1:n.*909C>A