Canonical Allele Identifier: CA413419091

Gene: VSIG4

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.66033772A>C , CM000685.2:g.66033772A>C	GRCh38
NC_000023.10:g.65253614A>C , CM000685.1:g.65253614A>C	GRCh37
NC_000023.9:g.65170339A>C	NCBI36
NG_021306.1:g.11354T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_007268.3:c.114T>G MANE Select	NP_009199.1:p.Asn38Lys
ENST00000374737.9:c.114T>G MANE Select	ENSP00000363869.4:p.Asn38Lys
NM_001100431.1:c.114T>G	NP_001093901.1:p.Asn38Lys
NM_001100431.2:c.114T>G	NP_001093901.1:p.Asn38Lys
NM_001184830.1:c.114T>G	NP_001171759.1:p.Asn38Lys
NM_001184830.2:c.114T>G	NP_001171759.1:p.Asn38Lys
NM_001184831.1:c.114T>G	NP_001171760.1:p.Asn38Lys
NM_001184831.2:c.114T>G	NP_001171760.1:p.Asn38Lys
NM_001257403.1:c.114T>G	NP_001244332.1:p.Asn38Lys
NM_001257403.2:c.114T>G	NP_001244332.1:p.Asn38Lys
NM_007268.2:c.114T>G	NP_009199.1:p.Asn38Lys
ENST00000374737.8:c.114T>G	ENSP00000363869.4:p.Asn38Lys
ENST00000412866.2:c.114T>G	ENSP00000394143.2:p.Asn38Lys
ENST00000455586.6:c.114T>G	ENSP00000411581.2:p.Asn38Lys
ENST00000651578.1:c.114T>G	ENSP00000498502.1:p.Asn38Lys
XM_017029251.2:c.114T>G	XP_016884740.1:p.Asn38Lys