Canonical Allele Identifier: CA384039685

Gene: MFAP5

Linked Data

• MyVariant Identifiers: chr12:g.8814655T>A (hg19) ; chr12:g.8662059T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8662059T>A , CM000674.2:g.8662059T>A	GRCh38
NC_000012.11:g.8814655T>A , CM000674.1:g.8814655T>A	GRCh37
NC_000012.10:g.8705922T>A	NCBI36
NG_041814.1:g.5830A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359478.7:c.46A>T MANE Select	ENSP00000352455.2:p.Ile16Phe
ENST00000359478.6:c.46A>T	ENSP00000352455.2:p.Ile16Phe
ENST00000396549.6:c.46A>T	ENSP00000379798.2:p.Ile16Phe
ENST00000433590.6:c.46A>T	ENSP00000411997.2:p.Ile16Phe
ENST00000534833.5:n.97A>T
ENST00000535336.5:c.46A>T	ENSP00000438525.1:p.Ile16Phe
ENST00000535411.5:c.15A>T
ENST00000537009.5:c.46A>T	ENSP00000439289.1:p.Ile16Phe
ENST00000537128.1:n.310A>T
ENST00000538107.5:n.310A>T
ENST00000540087.5:c.46A>T	ENSP00000440496.1:p.Ile16Phe
ENST00000543369.5:c.46A>T	ENSP00000441492.1:p.Ile16Phe
ENST00000544211.5:c.46A>T	ENSP00000443839.1:p.Ile16Phe
ENST00000544889.1:c.46A>T	ENSP00000445799.1:p.Ile16Phe
NM_001297709.1:c.46A>T	NP_001284638.1:p.Ile16Phe
NM_001297710.1:c.46A>T	NP_001284639.1:p.Ile16Phe
NM_001297711.1:c.46A>T	NP_001284640.1:p.Ile16Phe
NM_001297712.1:c.46A>T	NP_001284641.1:p.Ile16Phe
NM_003480.3:c.46A>T	NP_003471.1:p.Ile16Phe
NR_123733.1:n.310A>T
NR_123734.1:n.310A>T
NM_003480.4:c.46A>T MANE Select	NP_003471.1:p.Ile16Phe
NM_001297709.2:c.46A>T	NP_001284638.1:p.Ile16Phe
NM_001297710.2:c.46A>T	NP_001284639.1:p.Ile16Phe
NM_001297711.2:c.46A>T	NP_001284640.1:p.Ile16Phe
NM_001297712.2:c.46A>T	NP_001284641.1:p.Ile16Phe
NR_123733.2:n.248A>T
NR_123734.2:n.248A>T