Canonical Allele Identifier: CA2843056258

Gene: MFAP5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8648051C>T , CM000674.2:g.8648051C>T	GRCh38
NC_000012.11:g.8800647C>T , CM000674.1:g.8800647C>T	GRCh37
NC_000012.10:g.8691914C>T	NCBI36
NG_041814.1:g.19838G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359478.7:c.*40G>A MANE Select	ENSP00000352455.2:n.*40G>A
ENST00000359478.6:c.*40G>A	ENSP00000352455.2:n.*40G>A
ENST00000396549.6:c.*40G>A	ENSP00000379798.2:n.*40G>A
ENST00000433590.6:c.*40G>A	ENSP00000411997.2:n.*40G>A
ENST00000535336.5:c.*40G>A	ENSP00000438525.1:n.*40G>A
ENST00000535411.5:c.520+11G>A
ENST00000543369.5:c.*40G>A	ENSP00000441492.1:n.*40G>A
ENST00000543467.5:c.269+11G>A	ENSP00000444531.1:n.269+11G>A
ENST00000544211.5:c.*214G>A	ENSP00000443839.1:n.*214G>A
NM_001297709.1:c.*40G>A	NP_001284638.1:n.*40G>A
NM_001297710.1:c.*40G>A	NP_001284639.1:n.*40G>A
NM_001297711.1:c.*40G>A	NP_001284640.1:n.*40G>A
NM_001297712.1:c.*40G>A	NP_001284641.1:n.*40G>A
NM_003480.3:c.*40G>A	NP_003471.1:n.*40G>A
NR_123733.1:n.895G>A
NR_123734.1:n.865G>A
NM_003480.4:c.*40G>A MANE Select	NP_003471.1:n.*40G>A
NM_001297709.2:c.*40G>A	NP_001284638.1:n.*40G>A
NM_001297710.2:c.*40G>A	NP_001284639.1:n.*40G>A
NM_001297711.2:c.*40G>A	NP_001284640.1:n.*40G>A
NM_001297712.2:c.*40G>A	NP_001284641.1:n.*40G>A
NR_123733.2:n.833G>A
NR_123734.2:n.803G>A