Canonical Allele Identifier: CA2693938469
Gene: VSIG4 HGNC NCBI

Linked Data

gnomAD v4: X-66021920-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.66021920T>C , CM000685.2:g.66021920T>C GRCh38
NC_000023.10:g.65241762T>C , CM000685.1:g.65241762T>C GRCh37
NC_000023.9:g.65158487T>C NCBI36
NG_021306.1:g.23206A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000374737.9:c.*343A>G MANE Select ENSP00000363869.4:n.*343A>G
ENST00000651578.1:c.*793A>G ENSP00000498502.1:n.*793A>G
ENST00000374737.8:c.*343A>G ENSP00000363869.4:n.*343A>G
ENST00000412866.2:c.*343A>G ENSP00000394143.2:n.*343A>G
ENST00000427538.5:c.988A>G
ENST00000455586.6:c.*917A>G ENSP00000411581.2:n.*917A>G
NM_001100431.1:c.*343A>G NP_001093901.1:n.*343A>G
NM_001184830.1:c.*917A>G NP_001171759.1:n.*917A>G
NM_001184831.1:c.*917A>G NP_001171760.1:n.*917A>G
NM_001257403.1:c.*165A>G NP_001244332.1:n.*165A>G
NM_007268.2:c.*343A>G NP_009199.1:n.*343A>G
XM_017029251.2:c.*165A>G XP_016884740.1:n.*165A>G
NM_007268.3:c.*343A>G MANE Select NP_009199.1:n.*343A>G
NM_001100431.2:c.*343A>G NP_001093901.1:n.*343A>G
NM_001184831.2:c.*917A>G NP_001171760.1:n.*917A>G
NM_001257403.2:c.*165A>G NP_001244332.1:n.*165A>G
NM_001184830.2:c.*917A>G NP_001171759.1:n.*917A>G