Canonical Allele Identifier: CA431154998

Gene: FN1

Linked Data

• gnomAD v4: 2-215376592-C-G
• MyVariant Identifiers: chr2:g.216241315C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215376592C>G , CM000664.2:g.215376592C>G	GRCh38
NC_000002.11:g.216241315C>G , CM000664.1:g.216241315C>G	GRCh37
NC_000002.10:g.215949560C>G	NCBI36
NG_012196.1:g.64477G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354785.11:c.5793G>C MANE Select	ENSP00000346839.4:p.Thr1931=
ENST00000323926.10:c.5793G>C	ENSP00000323534.6:p.Thr1931=
ENST00000336916.8:c.5520G>C	ENSP00000338200.4:p.Thr1840=
ENST00000354785.8:c.5793G>C	ENSP00000346839.4:p.Thr1931=
ENST00000356005.8:c.5250G>C	ENSP00000348285.4:p.Thr1750=
ENST00000357867.8:c.5250G>C	ENSP00000350534.4:p.Thr1750=
ENST00000359671.5:c.5520G>C	ENSP00000352696.1:p.Thr1840=
ENST00000421182.5:c.5250G>C	ENSP00000394423.1:p.Thr1750=
ENST00000432072.6:c.5523G>C	ENSP00000399538.2:p.Thr1841=
ENST00000443816.5:c.5250G>C	ENSP00000415018.1:p.Thr1750=
ENST00000446046.5:c.5520G>C	ENSP00000410422.1:p.Thr1840=
ENST00000456923.5:c.1671G>C	ENSP00000416139.1:p.Thr557=
ENST00000474036.1:n.878G>C
ENST00000492816.6:n.6930G>C
NM_001306129.1:c.5793G>C	NP_001293058.1:p.Thr1931=
NM_001306130.1:c.5523G>C	NP_001293059.1:p.Thr1841=
NM_001306131.1:c.5250G>C	NP_001293060.1:p.Thr1750=
NM_001306132.1:c.5250G>C	NP_001293061.1:p.Thr1750=
NM_002026.2:c.5520G>C	NP_002017.1:p.Thr1840=
NM_212474.1:c.5250G>C	NP_997639.1:p.Thr1750=
NM_212476.1:c.5250G>C	NP_997641.1:p.Thr1750=
NM_212478.1:c.5520G>C	NP_997643.1:p.Thr1840=
NM_212482.1:c.5793G>C	NP_997647.1:p.Thr1931=
XM_005246397.1:c.5793G>C	XP_005246454.1:p.Thr1931=
XM_005246398.1:c.5793G>C	XP_005246455.1:p.Thr1931=
XM_005246399.1:c.5793G>C	XP_005246456.1:p.Thr1931=
XM_005246401.1:c.5793G>C	XP_005246458.1:p.Thr1931=
XM_005246402.1:c.5793G>C	XP_005246459.1:p.Thr1931=
XM_005246403.1:c.5523G>C	XP_005246460.1:p.Thr1841=
XM_005246404.1:c.5520G>C	XP_005246461.1:p.Thr1840=
XM_005246405.1:c.5523G>C	XP_005246462.1:p.Thr1841=
XM_005246406.1:c.5520G>C	XP_005246463.1:p.Thr1840=
XM_005246407.1:c.5793G>C	XP_005246464.1:p.Thr1931=
XM_005246408.1:c.5523G>C	XP_005246465.1:p.Thr1841=
XM_005246409.1:c.5520G>C	XP_005246466.1:p.Thr1840=
XM_005246410.1:c.5523G>C	XP_005246467.1:p.Thr1841=
XM_005246411.1:c.5523G>C	XP_005246468.1:p.Thr1841=
XM_005246412.1:c.5250G>C	XP_005246469.1:p.Thr1750=
XM_005246414.1:c.5520G>C	XP_005246471.1:p.Thr1840=
XM_005246416.1:c.5250G>C	XP_005246473.1:p.Thr1750=
NM_001365517.1:c.5523G>C	NP_001352446.1:p.Thr1841=
NM_001365518.1:c.5520G>C	NP_001352447.1:p.Thr1840=
NM_001365519.1:c.5523G>C	NP_001352448.1:p.Thr1841=
NM_001365520.1:c.5520G>C	NP_001352449.1:p.Thr1840=
NM_001365521.1:c.5523G>C	NP_001352450.1:p.Thr1841=
NM_001365522.1:c.5523G>C	NP_001352451.1:p.Thr1841=
NM_001365523.1:c.5250G>C	NP_001352452.1:p.Thr1750=
NM_001365524.1:c.5520G>C	NP_001352453.1:p.Thr1840=
NM_002026.3:c.5520G>C	NP_002017.1:p.Thr1840=
NM_212474.2:c.5250G>C	NP_997639.1:p.Thr1750=
NM_212476.2:c.5250G>C	NP_997641.1:p.Thr1750=
NM_212478.2:c.5520G>C	NP_997643.1:p.Thr1840=
NM_212482.2:c.5793G>C	NP_997647.1:p.Thr1931=
XM_017003692.1:c.5793G>C	XP_016859181.1:p.Thr1931=
XM_017003695.1:c.5250G>C	XP_016859184.1:p.Thr1750=
XM_024452769.1:c.5793G>C	XP_024308537.1:p.Thr1931=
XM_024452770.1:c.5523G>C	XP_024308538.1:p.Thr1841=
XR_002959450.1:n.132+3055C>G
NM_212482.3:c.5793G>C	NP_997647.1:p.Thr1931=
NM_001306129.2:c.5793G>C	NP_001293058.2:p.Thr1931=
NM_001306130.2:c.5523G>C	NP_001293059.2:p.Thr1841=
NM_001306131.2:c.5250G>C	NP_001293060.2:p.Thr1750=
NM_001306132.2:c.5250G>C	NP_001293061.2:p.Thr1750=
NM_001365517.2:c.5523G>C	NP_001352446.1:p.Thr1841=
NM_001365518.2:c.5520G>C	NP_001352447.1:p.Thr1840=
NM_001365519.2:c.5523G>C	NP_001352448.1:p.Thr1841=
NM_001365520.2:c.5520G>C	NP_001352449.1:p.Thr1840=
NM_001365521.2:c.5523G>C	NP_001352450.1:p.Thr1841=
NM_001365522.2:c.5523G>C	NP_001352451.1:p.Thr1841=
NM_001365523.2:c.5250G>C	NP_001352452.1:p.Thr1750=
NM_001365524.2:c.5520G>C	NP_001352453.1:p.Thr1840=
NM_002026.4:c.5520G>C	NP_002017.2:p.Thr1840=
NM_212474.3:c.5250G>C	NP_997639.2:p.Thr1750=
NM_212476.3:c.5250G>C	NP_997641.2:p.Thr1750=
NM_212478.3:c.5520G>C	NP_997643.2:p.Thr1840=
NM_212482.4:c.5793G>C MANE Select	NP_997647.2:p.Thr1931=