Canonical Allele Identifier: CA384038683

Gene: MFAP5

Linked Data

• MyVariant Identifiers: chr12:g.8800739A>G (hg19) ; chr12:g.8648143A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8648143A>G , CM000674.2:g.8648143A>G	GRCh38
NC_000012.11:g.8800739A>G , CM000674.1:g.8800739A>G	GRCh37
NC_000012.10:g.8692006A>G	NCBI36
NG_041814.1:g.19746T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359478.7:c.470T>C MANE Select	ENSP00000352455.2:p.Phe157Ser
ENST00000359478.6:c.470T>C	ENSP00000352455.2:p.Phe157Ser
ENST00000396549.6:c.440T>C	ENSP00000379798.2:p.Phe147Ser
ENST00000433590.6:c.395T>C	ENSP00000411997.2:p.Phe132Ser
ENST00000535336.5:c.278T>C	ENSP00000438525.1:p.Phe93Ser
ENST00000535411.5:c.439T>C
ENST00000537009.5:c.*122T>C	ENSP00000439289.1:n.*122T>C
ENST00000538694.5:n.429T>C
ENST00000540087.5:c.440T>C	ENSP00000440496.1:p.Phe147Ser
ENST00000543369.5:c.404T>C	ENSP00000441492.1:p.Phe135Ser
ENST00000543467.5:c.188T>C	ENSP00000444531.1:p.Phe63Ser
ENST00000544211.5:c.*122T>C	ENSP00000443839.1:n.*122T>C
NM_001297709.1:c.440T>C	NP_001284638.1:p.Phe147Ser
NM_001297710.1:c.404T>C	NP_001284639.1:p.Phe135Ser
NM_001297711.1:c.395T>C	NP_001284640.1:p.Phe132Ser
NM_001297712.1:c.278T>C	NP_001284641.1:p.Phe93Ser
NM_003480.3:c.470T>C	NP_003471.1:p.Phe157Ser
NR_123733.1:n.803T>C
NR_123734.1:n.773T>C
NM_003480.4:c.470T>C MANE Select	NP_003471.1:p.Phe157Ser
NM_001297709.2:c.440T>C	NP_001284638.1:p.Phe147Ser
NM_001297710.2:c.404T>C	NP_001284639.1:p.Phe135Ser
NM_001297711.2:c.395T>C	NP_001284640.1:p.Phe132Ser
NM_001297712.2:c.278T>C	NP_001284641.1:p.Phe93Ser
NR_123733.2:n.741T>C
NR_123734.2:n.711T>C