Canonical Allele Identifier: CA2697550436

Gene: FN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215361965T>G , CM000664.2:g.215361965T>G	GRCh38
NC_000002.11:g.216226688T>G , CM000664.1:g.216226688T>G	GRCh37
NC_000002.10:g.215934933T>G	NCBI36
NG_012196.1:g.79104A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354785.11:c.7362+4A>C MANE Select	ENSP00000346839.4:n.7362+4A>C
ENST00000323926.10:c.7269+4A>C	ENSP00000323534.6:n.7269+4A>C
ENST00000336916.8:c.6996+4A>C	ENSP00000338200.4:n.6996+4A>C
ENST00000354785.8:c.7362+4A>C	ENSP00000346839.4:n.7362+4A>C
ENST00000356005.8:c.6819+4A>C	ENSP00000348285.4:n.6819+4A>C
ENST00000357867.8:c.6459+4A>C	ENSP00000350534.4:n.6459+4A>C
ENST00000359671.5:c.7089+4A>C	ENSP00000352696.1:n.7089+4A>C
ENST00000421182.5:c.6651+4A>C	ENSP00000394423.1:n.6651+4A>C
ENST00000432072.6:c.6732+4A>C	ENSP00000399538.2:n.6732+4A>C
ENST00000443816.5:c.6726+4A>C	ENSP00000415018.1:n.6726+4A>C
ENST00000446046.5:c.6921+4A>C	ENSP00000410422.1:n.6921+4A>C
ENST00000456923.5:c.3240+4A>C	ENSP00000416139.1:n.3240+4A>C
ENST00000492816.6:n.8406+4A>C
ENST00000494446.1:n.390+4A>C
ENST00000498719.1:n.1672+4A>C
NM_001306129.1:c.7269+4A>C	NP_001293058.1:n.7269+4A>C
NM_001306130.1:c.6732+4A>C	NP_001293059.1:n.6732+4A>C
NM_001306131.1:c.6726+4A>C	NP_001293060.1:n.6726+4A>C
NM_001306132.1:c.6651+4A>C	NP_001293061.1:n.6651+4A>C
NM_002026.2:c.6996+4A>C	NP_002017.1:n.6996+4A>C
NM_212474.1:c.6459+4A>C	NP_997639.1:n.6459+4A>C
NM_212476.1:c.6819+4A>C	NP_997641.1:n.6819+4A>C
NM_212478.1:c.6921+4A>C	NP_997643.1:n.6921+4A>C
NM_212482.1:c.7362+4A>C	NP_997647.1:n.7362+4A>C
XM_005246397.1:c.7366A>C	XP_005246454.1:p.Ser2456Arg
XM_005246398.1:c.7291A>C	XP_005246455.1:p.Ser2431Arg
XM_005246399.1:c.7273A>C	XP_005246456.1:p.Ser2425Arg
XM_005246401.1:c.7198A>C	XP_005246458.1:p.Ser2400Arg
XM_005246402.1:c.7194+4A>C	XP_005246459.1:n.7194+4A>C
XM_005246403.1:c.7096A>C	XP_005246460.1:p.Ser2366Arg
XM_005246404.1:c.7093A>C	XP_005246461.1:p.Ser2365Arg
XM_005246405.1:c.7092+4A>C	XP_005246462.1:n.7092+4A>C
XM_005246406.1:c.7089+4A>C	XP_005246463.1:n.7089+4A>C
XM_005246407.1:c.7006A>C	XP_005246464.1:p.Ser2336Arg
XM_005246408.1:c.7003A>C	XP_005246465.1:p.Ser2335Arg
XM_005246409.1:c.7014+4A>C	XP_005246466.1:n.7014+4A>C
XM_005246410.1:c.6928A>C	XP_005246467.1:p.Ser2310Arg
XM_005246411.1:c.6736A>C	XP_005246468.1:p.Ser2246Arg
XM_005246412.1:c.6744+4A>C	XP_005246469.1:n.6744+4A>C
XM_005246414.1:c.6729+4A>C	XP_005246471.1:n.6729+4A>C
XM_005246416.1:c.6655A>C	XP_005246473.1:p.Ser2219Arg
XR_923860.1:n.222-681T>G
XR_923861.1:n.1130-681T>G
NM_001365517.1:c.7092+4A>C	NP_001352446.1:n.7092+4A>C
NM_001365518.1:c.7089+4A>C	NP_001352447.1:n.7089+4A>C
NM_001365519.1:c.7017+4A>C	NP_001352448.1:n.7017+4A>C
NM_001365520.1:c.7014+4A>C	NP_001352449.1:n.7014+4A>C
NM_001365521.1:c.6999+4A>C	NP_001352450.1:n.6999+4A>C
NM_001365522.1:c.6924+4A>C	NP_001352451.1:n.6924+4A>C
NM_001365523.1:c.6744+4A>C	NP_001352452.1:n.6744+4A>C
NM_001365524.1:c.6729+4A>C	NP_001352453.1:n.6729+4A>C
NM_002026.3:c.6996+4A>C	NP_002017.1:n.6996+4A>C
NM_212474.2:c.6459+4A>C	NP_997639.1:n.6459+4A>C
NM_212476.2:c.6819+4A>C	NP_997641.1:n.6819+4A>C
NM_212478.2:c.6921+4A>C	NP_997643.1:n.6921+4A>C
NM_212482.2:c.7362+4A>C	NP_997647.1:n.7362+4A>C
XM_017003692.1:c.7002+4A>C	XP_016859181.1:n.7002+4A>C
XM_017003695.1:c.6823A>C	XP_016859184.1:p.Ser2275Arg
XM_024452769.1:c.7287+4A>C	XP_024308537.1:n.7287+4A>C
XM_024452770.1:c.7021A>C	XP_024308538.1:p.Ser2341Arg
NM_212482.3:c.7362+4A>C	NP_997647.1:n.7362+4A>C
NM_001306129.2:c.7269+4A>C	NP_001293058.2:n.7269+4A>C
NM_001306130.2:c.6732+4A>C	NP_001293059.2:n.6732+4A>C
NM_001306131.2:c.6726+4A>C	NP_001293060.2:n.6726+4A>C
NM_001306132.2:c.6651+4A>C	NP_001293061.2:n.6651+4A>C
NM_001365517.2:c.7092+4A>C	NP_001352446.1:n.7092+4A>C
NM_001365518.2:c.7089+4A>C	NP_001352447.1:n.7089+4A>C
NM_001365519.2:c.7017+4A>C	NP_001352448.1:n.7017+4A>C
NM_001365520.2:c.7014+4A>C	NP_001352449.1:n.7014+4A>C
NM_001365521.2:c.6999+4A>C	NP_001352450.1:n.6999+4A>C
NM_001365522.2:c.6924+4A>C	NP_001352451.1:n.6924+4A>C
NM_001365523.2:c.6744+4A>C	NP_001352452.1:n.6744+4A>C
NM_001365524.2:c.6729+4A>C	NP_001352453.1:n.6729+4A>C
NM_002026.4:c.6996+4A>C	NP_002017.2:n.6996+4A>C
NM_212474.3:c.6459+4A>C	NP_997639.2:n.6459+4A>C
NM_212476.3:c.6819+4A>C	NP_997641.2:n.6819+4A>C
NM_212478.3:c.6921+4A>C	NP_997643.2:n.6921+4A>C
NM_212482.4:c.7362+4A>C MANE Select	NP_997647.2:n.7362+4A>C