Canonical Allele Identifier: CA2580065631

Gene: FN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215364874C>A , CM000664.2:g.215364874C>A	GRCh38
NC_000002.11:g.216229597C>A , CM000664.1:g.216229597C>A	GRCh37
NC_000002.10:g.215937842C>A	NCBI36
NG_012196.1:g.76195G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354785.11:c.7251+5G>T MANE Select	ENSP00000346839.4:n.7251+5G>T
ENST00000323926.10:c.7158+5G>T	ENSP00000323534.6:n.7158+5G>T
ENST00000336916.8:c.6885+5G>T	ENSP00000338200.4:n.6885+5G>T
ENST00000354785.8:c.7251+5G>T	ENSP00000346839.4:n.7251+5G>T
ENST00000356005.8:c.6708+5G>T	ENSP00000348285.4:n.6708+5G>T
ENST00000357867.8:c.6348+5G>T	ENSP00000350534.4:n.6348+5G>T
ENST00000359671.5:c.6978+5G>T	ENSP00000352696.1:n.6978+5G>T
ENST00000421182.5:c.6540+5G>T	ENSP00000394423.1:n.6540+5G>T
ENST00000432072.6:c.6621+5G>T	ENSP00000399538.2:n.6621+5G>T
ENST00000443816.5:c.6615+5G>T	ENSP00000415018.1:n.6615+5G>T
ENST00000446046.5:c.6810+5G>T	ENSP00000410422.1:n.6810+5G>T
ENST00000456923.5:c.3129+5G>T	ENSP00000416139.1:n.3129+5G>T
ENST00000469569.1:n.125G>T
ENST00000473614.1:n.361G>T
ENST00000492816.6:n.8295+5G>T
ENST00000494446.1:n.279+5G>T
NM_001306129.1:c.7158+5G>T	NP_001293058.1:n.7158+5G>T
NM_001306130.1:c.6621+5G>T	NP_001293059.1:n.6621+5G>T
NM_001306131.1:c.6615+5G>T	NP_001293060.1:n.6615+5G>T
NM_001306132.1:c.6540+5G>T	NP_001293061.1:n.6540+5G>T
NM_002026.2:c.6885+5G>T	NP_002017.1:n.6885+5G>T
NM_212474.1:c.6348+5G>T	NP_997639.1:n.6348+5G>T
NM_212476.1:c.6708+5G>T	NP_997641.1:n.6708+5G>T
NM_212478.1:c.6810+5G>T	NP_997643.1:n.6810+5G>T
NM_212482.1:c.7251+5G>T	NP_997647.1:n.7251+5G>T
XM_005246397.1:c.7251+5G>T	XP_005246454.1:n.7251+5G>T
XM_005246398.1:c.7176+5G>T	XP_005246455.1:n.7176+5G>T
XM_005246399.1:c.7158+5G>T	XP_005246456.1:n.7158+5G>T
XM_005246401.1:c.7083+5G>T	XP_005246458.1:n.7083+5G>T
XM_005246402.1:c.7083+5G>T	XP_005246459.1:n.7083+5G>T
XM_005246403.1:c.6981+5G>T	XP_005246460.1:n.6981+5G>T
XM_005246404.1:c.6978+5G>T	XP_005246461.1:n.6978+5G>T
XM_005246405.1:c.6981+5G>T	XP_005246462.1:n.6981+5G>T
XM_005246406.1:c.6978+5G>T	XP_005246463.1:n.6978+5G>T
XM_005246407.1:c.6891+5G>T	XP_005246464.1:n.6891+5G>T
XM_005246408.1:c.6888+5G>T	XP_005246465.1:n.6888+5G>T
XM_005246409.1:c.6903+5G>T	XP_005246466.1:n.6903+5G>T
XM_005246410.1:c.6813+5G>T	XP_005246467.1:n.6813+5G>T
XM_005246411.1:c.6621+5G>T	XP_005246468.1:n.6621+5G>T
XM_005246412.1:c.6633+5G>T	XP_005246469.1:n.6633+5G>T
XM_005246414.1:c.6618+5G>T	XP_005246471.1:n.6618+5G>T
XM_005246416.1:c.6540+5G>T	XP_005246473.1:n.6540+5G>T
NM_001365517.1:c.6981+5G>T	NP_001352446.1:n.6981+5G>T
NM_001365518.1:c.6978+5G>T	NP_001352447.1:n.6978+5G>T
NM_001365519.1:c.6906+5G>T	NP_001352448.1:n.6906+5G>T
NM_001365520.1:c.6903+5G>T	NP_001352449.1:n.6903+5G>T
NM_001365521.1:c.6888+5G>T	NP_001352450.1:n.6888+5G>T
NM_001365522.1:c.6813+5G>T	NP_001352451.1:n.6813+5G>T
NM_001365523.1:c.6633+5G>T	NP_001352452.1:n.6633+5G>T
NM_001365524.1:c.6618+5G>T	NP_001352453.1:n.6618+5G>T
NM_002026.3:c.6885+5G>T	NP_002017.1:n.6885+5G>T
NM_212474.2:c.6348+5G>T	NP_997639.1:n.6348+5G>T
NM_212476.2:c.6708+5G>T	NP_997641.1:n.6708+5G>T
NM_212478.2:c.6810+5G>T	NP_997643.1:n.6810+5G>T
NM_212482.2:c.7251+5G>T	NP_997647.1:n.7251+5G>T
XM_017003692.1:c.6891+5G>T	XP_016859181.1:n.6891+5G>T
XM_017003695.1:c.6708+5G>T	XP_016859184.1:n.6708+5G>T
XM_024452769.1:c.7176+5G>T	XP_024308537.1:n.7176+5G>T
XM_024452770.1:c.6906+5G>T	XP_024308538.1:n.6906+5G>T
NM_212482.3:c.7251+5G>T	NP_997647.1:n.7251+5G>T
NM_001306129.2:c.7158+5G>T	NP_001293058.2:n.7158+5G>T
NM_001306130.2:c.6621+5G>T	NP_001293059.2:n.6621+5G>T
NM_001306131.2:c.6615+5G>T	NP_001293060.2:n.6615+5G>T
NM_001306132.2:c.6540+5G>T	NP_001293061.2:n.6540+5G>T
NM_001365517.2:c.6981+5G>T	NP_001352446.1:n.6981+5G>T
NM_001365518.2:c.6978+5G>T	NP_001352447.1:n.6978+5G>T
NM_001365519.2:c.6906+5G>T	NP_001352448.1:n.6906+5G>T
NM_001365520.2:c.6903+5G>T	NP_001352449.1:n.6903+5G>T
NM_001365521.2:c.6888+5G>T	NP_001352450.1:n.6888+5G>T
NM_001365522.2:c.6813+5G>T	NP_001352451.1:n.6813+5G>T
NM_001365523.2:c.6633+5G>T	NP_001352452.1:n.6633+5G>T
NM_001365524.2:c.6618+5G>T	NP_001352453.1:n.6618+5G>T
NM_002026.4:c.6885+5G>T	NP_002017.2:n.6885+5G>T
NM_212474.3:c.6348+5G>T	NP_997639.2:n.6348+5G>T
NM_212476.3:c.6708+5G>T	NP_997641.2:n.6708+5G>T
NM_212478.3:c.6810+5G>T	NP_997643.2:n.6810+5G>T
NM_212482.4:c.7251+5G>T MANE Select	NP_997647.2:n.7251+5G>T