Canonical Allele Identifier: CA2015131037

Gene: MFAP5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8648155C= , CM000674.2:g.8648155C=	GRCh38
NC_000012.11:g.8800751C= , CM000674.1:g.8800751C=	GRCh37
NC_000012.10:g.8692018C=	NCBI36
NG_041814.1:g.19734G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359478.7:c.458G= MANE Select	ENSP00000352455.2:p.Arg153=
ENST00000359478.6:c.458G=	ENSP00000352455.2:p.Arg153=
ENST00000396549.6:c.428G=	ENSP00000379798.2:p.Arg143=
ENST00000433590.6:c.383G=	ENSP00000411997.2:p.Arg128=
ENST00000535336.5:c.266G=	ENSP00000438525.1:p.Arg89=
ENST00000535411.5:c.427G=
ENST00000537009.5:c.*110G=	ENSP00000439289.1:n.*110G=
ENST00000538694.5:n.417G=
ENST00000540087.5:c.428G=	ENSP00000440496.1:p.Arg143=
ENST00000543369.5:c.392G=	ENSP00000441492.1:p.Arg131=
ENST00000543467.5:c.176G=	ENSP00000444531.1:p.Arg59=
ENST00000544211.5:c.*110G=	ENSP00000443839.1:n.*110G=
NM_001297709.1:c.428G=	NP_001284638.1:p.Arg143=
NM_001297710.1:c.392G=	NP_001284639.1:p.Arg131=
NM_001297711.1:c.383G=	NP_001284640.1:p.Arg128=
NM_001297712.1:c.266G=	NP_001284641.1:p.Arg89=
NM_003480.3:c.458G=	NP_003471.1:p.Arg153=
NR_123733.1:n.791G=
NR_123734.1:n.761G=
NM_003480.4:c.458G= MANE Select	NP_003471.1:p.Arg153=
NM_001297709.2:c.428G=	NP_001284638.1:p.Arg143=
NM_001297710.2:c.392G=	NP_001284639.1:p.Arg131=
NM_001297711.2:c.383G=	NP_001284640.1:p.Arg128=
NM_001297712.2:c.266G=	NP_001284641.1:p.Arg89=
NR_123733.2:n.729G=
NR_123734.2:n.699G=