Canonical Allele Identifier: CA2015131034

Gene: MFAP5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8648149T= , CM000674.2:g.8648149T=	GRCh38
NC_000012.11:g.8800745T= , CM000674.1:g.8800745T=	GRCh37
NC_000012.10:g.8692012T=	NCBI36
NG_041814.1:g.19740A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359478.7:c.464A= MANE Select	ENSP00000352455.2:p.Asn155=
ENST00000359478.6:c.464A=	ENSP00000352455.2:p.Asn155=
ENST00000396549.6:c.434A=	ENSP00000379798.2:p.Asn145=
ENST00000433590.6:c.389A=	ENSP00000411997.2:p.Asn130=
ENST00000535336.5:c.272A=	ENSP00000438525.1:p.Asn91=
ENST00000535411.5:c.433A=
ENST00000537009.5:c.*116A=	ENSP00000439289.1:n.*116A=
ENST00000538694.5:n.423A=
ENST00000540087.5:c.434A=	ENSP00000440496.1:p.Asn145=
ENST00000543369.5:c.398A=	ENSP00000441492.1:p.Asn133=
ENST00000543467.5:c.182A=	ENSP00000444531.1:p.Asn61=
ENST00000544211.5:c.*116A=	ENSP00000443839.1:n.*116A=
NM_001297709.1:c.434A=	NP_001284638.1:p.Asn145=
NM_001297710.1:c.398A=	NP_001284639.1:p.Asn133=
NM_001297711.1:c.389A=	NP_001284640.1:p.Asn130=
NM_001297712.1:c.272A=	NP_001284641.1:p.Asn91=
NM_003480.3:c.464A=	NP_003471.1:p.Asn155=
NR_123733.1:n.797A=
NR_123734.1:n.767A=
NM_003480.4:c.464A= MANE Select	NP_003471.1:p.Asn155=
NM_001297709.2:c.434A=	NP_001284638.1:p.Asn145=
NM_001297710.2:c.398A=	NP_001284639.1:p.Asn133=
NM_001297711.2:c.389A=	NP_001284640.1:p.Asn130=
NM_001297712.2:c.272A=	NP_001284641.1:p.Asn91=
NR_123733.2:n.735A=
NR_123734.2:n.705A=