Canonical Allele Identifier: CA2015131033

Gene: MFAP5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8648141G= , CM000674.2:g.8648141G=	GRCh38
NC_000012.11:g.8800737G= , CM000674.1:g.8800737G=	GRCh37
NC_000012.10:g.8692004G=	NCBI36
NG_041814.1:g.19748C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359478.7:c.472C= MANE Select	ENSP00000352455.2:p.Arg158=
ENST00000359478.6:c.472C=	ENSP00000352455.2:p.Arg158=
ENST00000396549.6:c.442C=	ENSP00000379798.2:p.Arg148=
ENST00000433590.6:c.397C=	ENSP00000411997.2:p.Arg133=
ENST00000535336.5:c.280C=	ENSP00000438525.1:p.Arg94=
ENST00000535411.5:c.441C=
ENST00000537009.5:c.*124C=	ENSP00000439289.1:n.*124C=
ENST00000538694.5:n.431C=
ENST00000540087.5:c.442C=	ENSP00000440496.1:p.Arg148=
ENST00000543369.5:c.406C=	ENSP00000441492.1:p.Arg136=
ENST00000543467.5:c.190C=	ENSP00000444531.1:p.Arg64=
ENST00000544211.5:c.*124C=	ENSP00000443839.1:n.*124C=
NM_001297709.1:c.442C=	NP_001284638.1:p.Arg148=
NM_001297710.1:c.406C=	NP_001284639.1:p.Arg136=
NM_001297711.1:c.397C=	NP_001284640.1:p.Arg133=
NM_001297712.1:c.280C=	NP_001284641.1:p.Arg94=
NM_003480.3:c.472C=	NP_003471.1:p.Arg158=
NR_123733.1:n.805C=
NR_123734.1:n.775C=
NM_003480.4:c.472C= MANE Select	NP_003471.1:p.Arg158=
NM_001297709.2:c.442C=	NP_001284638.1:p.Arg148=
NM_001297710.2:c.406C=	NP_001284639.1:p.Arg136=
NM_001297711.2:c.397C=	NP_001284640.1:p.Arg133=
NM_001297712.2:c.280C=	NP_001284641.1:p.Arg94=
NR_123733.2:n.743C=
NR_123734.2:n.713C=