Canonical Allele Identifier: CA2015131035
Gene: MFAP5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8648152G= , CM000674.2:g.8648152G= GRCh38
NC_000012.11:g.8800748G= , CM000674.1:g.8800748G= GRCh37
NC_000012.10:g.8692015G= NCBI36
NG_041814.1:g.19737C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000359478.7:c.461C= MANE Select ENSP00000352455.2:p.Ser154=
ENST00000359478.6:c.461C= ENSP00000352455.2:p.Ser154=
ENST00000396549.6:c.431C= ENSP00000379798.2:p.Ser144=
ENST00000433590.6:c.386C= ENSP00000411997.2:p.Ser129=
ENST00000535336.5:c.269C= ENSP00000438525.1:p.Ser90=
ENST00000535411.5:c.430C=
ENST00000537009.5:c.*113C= ENSP00000439289.1:n.*113C=
ENST00000538694.5:n.420C=
ENST00000540087.5:c.431C= ENSP00000440496.1:p.Ser144=
ENST00000543369.5:c.395C= ENSP00000441492.1:p.Ser132=
ENST00000543467.5:c.179C= ENSP00000444531.1:p.Ser60=
ENST00000544211.5:c.*113C= ENSP00000443839.1:n.*113C=
NM_001297709.1:c.431C= NP_001284638.1:p.Ser144=
NM_001297710.1:c.395C= NP_001284639.1:p.Ser132=
NM_001297711.1:c.386C= NP_001284640.1:p.Ser129=
NM_001297712.1:c.269C= NP_001284641.1:p.Ser90=
NM_003480.3:c.461C= NP_003471.1:p.Ser154=
NR_123733.1:n.794C=
NR_123734.1:n.764C=
NM_003480.4:c.461C= MANE Select NP_003471.1:p.Ser154=
NM_001297709.2:c.431C= NP_001284638.1:p.Ser144=
NM_001297710.2:c.395C= NP_001284639.1:p.Ser132=
NM_001297711.2:c.386C= NP_001284640.1:p.Ser129=
NM_001297712.2:c.269C= NP_001284641.1:p.Ser90=
NR_123733.2:n.732C=
NR_123734.2:n.702C=