Canonical Allele Identifier: CA2434248673

Gene: VSIG4

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.66021886_66021887delinsTA , CM000685.2:g.66021886_66021887delinsTA	GRCh38
NC_000023.10:g.65241728_65241729delinsTA , CM000685.1:g.65241728_65241729delinsTA	GRCh37
NC_000023.9:g.65158453_65158454delinsTA	NCBI36
NG_021306.1:g.23239_23240delinsTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000374737.9:c.*376_*377delinsTA MANE Select	ENSP00000363869.4:n.*376_*377delinsTA
ENST00000651578.1:c.*826_*827delinsTA	ENSP00000498502.1:n.*826_*827delinsTA
ENST00000374737.8:c.*376_*377delinsTA	ENSP00000363869.4:n.*376_*377delinsTA
ENST00000412866.2:c.*376_*377delinsTA	ENSP00000394143.2:n.*376_*377delinsTA
ENST00000427538.5:c.1021_1022delinsTA
ENST00000455586.6:c.*950_*951delinsTA	ENSP00000411581.2:n.*950_*951delinsTA
NM_001100431.1:c.*376_*377delinsTA	NP_001093901.1:n.*376_*377delinsTA
NM_001184830.1:c.*950_*951delinsTA	NP_001171759.1:n.*950_*951delinsTA
NM_001184831.1:c.*950_*951delinsTA	NP_001171760.1:n.*950_*951delinsTA
NM_001257403.1:c.*198_*199delinsTA	NP_001244332.1:n.*198_*199delinsTA
NM_007268.2:c.*376_*377delinsTA	NP_009199.1:n.*376_*377delinsTA
XM_017029251.2:c.*198_*199delinsTA	XP_016884740.1:n.*198_*199delinsTA
NM_007268.3:c.*376_*377delinsTA MANE Select	NP_009199.1:n.*376_*377delinsTA
NM_001100431.2:c.*376_*377delinsTA	NP_001093901.1:n.*376_*377delinsTA
NM_001184831.2:c.*950_*951delinsTA	NP_001171760.1:n.*950_*951delinsTA
NM_001257403.2:c.*198_*199delinsTA	NP_001244332.1:n.*198_*199delinsTA
NM_001184830.2:c.*950_*951delinsTA	NP_001171759.1:n.*950_*951delinsTA