Canonical Allele Identifier: CA2093660

Gene: FN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215365573C>A , CM000664.2:g.215365573C>A	GRCh38
NC_000002.11:g.216230296C>A , CM000664.1:g.216230296C>A	GRCh37
NC_000002.10:g.215938541C>A	NCBI36
NG_012196.1:g.75496G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354785.11:c.7076G>T MANE Select	ENSP00000346839.4:p.Gly2359Val
ENST00000323926.10:c.6983G>T	ENSP00000323534.6:p.Gly2328Val
ENST00000336916.8:c.6710G>T	ENSP00000338200.4:p.Gly2237Val
ENST00000354785.8:c.7076G>T	ENSP00000346839.4:p.Gly2359Val
ENST00000356005.8:c.6533G>T	ENSP00000348285.4:p.Gly2178Val
ENST00000357867.8:c.6173G>T	ENSP00000350534.4:p.Gly2058Val
ENST00000359671.5:c.6803G>T	ENSP00000352696.1:p.Gly2268Val
ENST00000421182.5:c.6365G>T	ENSP00000394423.1:p.Gly2122Val
ENST00000432072.6:c.6446G>T	ENSP00000399538.2:p.Gly2149Val
ENST00000443816.5:c.6440G>T	ENSP00000415018.1:p.Gly2147Val
ENST00000446046.5:c.6635G>T	ENSP00000410422.1:p.Gly2212Val
ENST00000456923.5:c.2954G>T	ENSP00000416139.1:p.Gly985Val
ENST00000473614.1:n.181G>T
ENST00000492816.6:n.8120G>T
ENST00000494446.1:n.104G>T
NM_001306129.1:c.6983G>T	NP_001293058.1:p.Gly2328Val
NM_001306130.1:c.6446G>T	NP_001293059.1:p.Gly2149Val
NM_001306131.1:c.6440G>T	NP_001293060.1:p.Gly2147Val
NM_001306132.1:c.6365G>T	NP_001293061.1:p.Gly2122Val
NM_002026.2:c.6710G>T	NP_002017.1:p.Gly2237Val
NM_212474.1:c.6173G>T	NP_997639.1:p.Gly2058Val
NM_212476.1:c.6533G>T	NP_997641.1:p.Gly2178Val
NM_212478.1:c.6635G>T	NP_997643.1:p.Gly2212Val
NM_212482.1:c.7076G>T	NP_997647.1:p.Gly2359Val
XM_005246397.1:c.7076G>T	XP_005246454.1:p.Gly2359Val
XM_005246398.1:c.7001G>T	XP_005246455.1:p.Gly2334Val
XM_005246399.1:c.6983G>T	XP_005246456.1:p.Gly2328Val
XM_005246401.1:c.6908G>T	XP_005246458.1:p.Gly2303Val
XM_005246402.1:c.6908G>T	XP_005246459.1:p.Gly2303Val
XM_005246403.1:c.6806G>T	XP_005246460.1:p.Gly2269Val
XM_005246404.1:c.6803G>T	XP_005246461.1:p.Gly2268Val
XM_005246405.1:c.6806G>T	XP_005246462.1:p.Gly2269Val
XM_005246406.1:c.6803G>T	XP_005246463.1:p.Gly2268Val
XM_005246407.1:c.6716G>T	XP_005246464.1:p.Gly2239Val
XM_005246408.1:c.6713G>T	XP_005246465.1:p.Gly2238Val
XM_005246409.1:c.6728G>T	XP_005246466.1:p.Gly2243Val
XM_005246410.1:c.6638G>T	XP_005246467.1:p.Gly2213Val
XM_005246411.1:c.6446G>T	XP_005246468.1:p.Gly2149Val
XM_005246412.1:c.6458G>T	XP_005246469.1:p.Gly2153Val
XM_005246414.1:c.6443G>T	XP_005246471.1:p.Gly2148Val
XM_005246416.1:c.6365G>T	XP_005246473.1:p.Gly2122Val
NM_001365517.1:c.6806G>T	NP_001352446.1:p.Gly2269Val
NM_001365518.1:c.6803G>T	NP_001352447.1:p.Gly2268Val
NM_001365519.1:c.6731G>T	NP_001352448.1:p.Gly2244Val
NM_001365520.1:c.6728G>T	NP_001352449.1:p.Gly2243Val
NM_001365521.1:c.6713G>T	NP_001352450.1:p.Gly2238Val
NM_001365522.1:c.6638G>T	NP_001352451.1:p.Gly2213Val
NM_001365523.1:c.6458G>T	NP_001352452.1:p.Gly2153Val
NM_001365524.1:c.6443G>T	NP_001352453.1:p.Gly2148Val
NM_002026.3:c.6710G>T	NP_002017.1:p.Gly2237Val
NM_212474.2:c.6173G>T	NP_997639.1:p.Gly2058Val
NM_212476.2:c.6533G>T	NP_997641.1:p.Gly2178Val
NM_212478.2:c.6635G>T	NP_997643.1:p.Gly2212Val
NM_212482.2:c.7076G>T	NP_997647.1:p.Gly2359Val
XM_017003692.1:c.6716G>T	XP_016859181.1:p.Gly2239Val
XM_017003695.1:c.6533G>T	XP_016859184.1:p.Gly2178Val
XM_024452769.1:c.7001G>T	XP_024308537.1:p.Gly2334Val
XM_024452770.1:c.6731G>T	XP_024308538.1:p.Gly2244Val
NM_212482.3:c.7076G>T	NP_997647.1:p.Gly2359Val
NM_001306129.2:c.6983G>T	NP_001293058.2:p.Gly2328Val
NM_001306130.2:c.6446G>T	NP_001293059.2:p.Gly2149Val
NM_001306131.2:c.6440G>T	NP_001293060.2:p.Gly2147Val
NM_001306132.2:c.6365G>T	NP_001293061.2:p.Gly2122Val
NM_001365517.2:c.6806G>T	NP_001352446.1:p.Gly2269Val
NM_001365518.2:c.6803G>T	NP_001352447.1:p.Gly2268Val
NM_001365519.2:c.6731G>T	NP_001352448.1:p.Gly2244Val
NM_001365520.2:c.6728G>T	NP_001352449.1:p.Gly2243Val
NM_001365521.2:c.6713G>T	NP_001352450.1:p.Gly2238Val
NM_001365522.2:c.6638G>T	NP_001352451.1:p.Gly2213Val
NM_001365523.2:c.6458G>T	NP_001352452.1:p.Gly2153Val
NM_001365524.2:c.6443G>T	NP_001352453.1:p.Gly2148Val
NM_002026.4:c.6710G>T	NP_002017.2:p.Gly2237Val
NM_212474.3:c.6173G>T	NP_997639.2:p.Gly2058Val
NM_212476.3:c.6533G>T	NP_997641.2:p.Gly2178Val
NM_212478.3:c.6635G>T	NP_997643.2:p.Gly2212Val
NM_212482.4:c.7076G>T MANE Select	NP_997647.2:p.Gly2359Val