Canonical Allele Identifier: CA2617498710

Gene: MFAP5

Linked Data

• gnomAD v4: 12-8648070-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8648070T>C , CM000674.2:g.8648070T>C	GRCh38
NC_000012.11:g.8800666T>C , CM000674.1:g.8800666T>C	GRCh37
NC_000012.10:g.8691933T>C	NCBI36
NG_041814.1:g.19819A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359478.7:c.*21A>G MANE Select	ENSP00000352455.2:n.*21A>G
ENST00000359478.6:c.*21A>G	ENSP00000352455.2:n.*21A>G
ENST00000396549.6:c.*21A>G	ENSP00000379798.2:n.*21A>G
ENST00000433590.6:c.*21A>G	ENSP00000411997.2:n.*21A>G
ENST00000535336.5:c.*21A>G	ENSP00000438525.1:n.*21A>G
ENST00000535411.5:c.512A>G
ENST00000543369.5:c.*21A>G	ENSP00000441492.1:n.*21A>G
ENST00000543467.5:c.261A>G	ENSP00000444531.1:n.261A>G
ENST00000544211.5:c.*195A>G	ENSP00000443839.1:n.*195A>G
NM_001297709.1:c.*21A>G	NP_001284638.1:n.*21A>G
NM_001297710.1:c.*21A>G	NP_001284639.1:n.*21A>G
NM_001297711.1:c.*21A>G	NP_001284640.1:n.*21A>G
NM_001297712.1:c.*21A>G	NP_001284641.1:n.*21A>G
NM_003480.3:c.*21A>G	NP_003471.1:n.*21A>G
NR_123733.1:n.876A>G
NR_123734.1:n.846A>G
NM_003480.4:c.*21A>G MANE Select	NP_003471.1:n.*21A>G
NM_001297709.2:c.*21A>G	NP_001284638.1:n.*21A>G
NM_001297710.2:c.*21A>G	NP_001284639.1:n.*21A>G
NM_001297711.2:c.*21A>G	NP_001284640.1:n.*21A>G
NM_001297712.2:c.*21A>G	NP_001284641.1:n.*21A>G
NR_123733.2:n.814A>G
NR_123734.2:n.784A>G