Canonical Allele Identifier: CA2015130949

Gene: MFAP5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8648062A= , CM000674.2:g.8648062A=	GRCh38
NC_000012.11:g.8800658A= , CM000674.1:g.8800658A=	GRCh37
NC_000012.10:g.8691925A=	NCBI36
NG_041814.1:g.19827T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359478.7:c.*29T= MANE Select	ENSP00000352455.2:n.*29T=
ENST00000359478.6:c.*29T=	ENSP00000352455.2:n.*29T=
ENST00000396549.6:c.*29T=	ENSP00000379798.2:n.*29T=
ENST00000433590.6:c.*29T=	ENSP00000411997.2:n.*29T=
ENST00000535336.5:c.*29T=	ENSP00000438525.1:n.*29T=
ENST00000535411.5:c.520T=
ENST00000543369.5:c.*29T=	ENSP00000441492.1:n.*29T=
ENST00000543467.5:c.269T=	ENSP00000444531.1:n.269T=
ENST00000544211.5:c.*203T=	ENSP00000443839.1:n.*203T=
NM_001297709.1:c.*29T=	NP_001284638.1:n.*29T=
NM_001297710.1:c.*29T=	NP_001284639.1:n.*29T=
NM_001297711.1:c.*29T=	NP_001284640.1:n.*29T=
NM_001297712.1:c.*29T=	NP_001284641.1:n.*29T=
NM_003480.3:c.*29T=	NP_003471.1:n.*29T=
NR_123733.1:n.884T=
NR_123734.1:n.854T=
NM_003480.4:c.*29T= MANE Select	NP_003471.1:n.*29T=
NM_001297709.2:c.*29T=	NP_001284638.1:n.*29T=
NM_001297710.2:c.*29T=	NP_001284639.1:n.*29T=
NM_001297711.2:c.*29T=	NP_001284640.1:n.*29T=
NM_001297712.2:c.*29T=	NP_001284641.1:n.*29T=
NR_123733.2:n.822T=
NR_123734.2:n.792T=