Canonical Allele Identifier: CA204749
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 208716
ClinVar RCV Id: RCV000190733
dbSNP Id: rs797044906
MyVariant Identifiers: chr2:g.216269314C>A (hg19) chr2:g.215404591C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215404591C>A , CM000664.2:g.215404591C>A GRCh38
NC_000002.11:g.216269314C>A , CM000664.1:g.216269314C>A GRCh37
NC_000002.10:g.215977559C>A NCBI36
NG_012196.1:g.36478G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000354785.11:c.3051G>T MANE Select ENSP00000346839.4:p.Trp1017Cys
ENST00000323926.10:c.3051G>T ENSP00000323534.6:p.Trp1017Cys
ENST00000336916.8:c.3051G>T ENSP00000338200.4:p.Trp1017Cys
ENST00000354785.8:c.3051G>T ENSP00000346839.4:p.Trp1017Cys
ENST00000356005.8:c.3051G>T ENSP00000348285.4:p.Trp1017Cys
ENST00000357867.8:c.3051G>T ENSP00000350534.4:p.Trp1017Cys
ENST00000359671.5:c.3051G>T ENSP00000352696.1:p.Trp1017Cys
ENST00000421182.5:c.3051G>T ENSP00000394423.1:p.Trp1017Cys
ENST00000432072.6:c.3051G>T ENSP00000399538.2:p.Trp1017Cys
ENST00000443816.5:c.3051G>T ENSP00000415018.1:p.Trp1017Cys
ENST00000446046.5:c.3051G>T ENSP00000410422.1:p.Trp1017Cys
NM_001306129.1:c.3051G>T NP_001293058.1:p.Trp1017Cys
NM_001306130.1:c.3051G>T NP_001293059.1:p.Trp1017Cys
NM_001306131.1:c.3051G>T NP_001293060.1:p.Trp1017Cys
NM_001306132.1:c.3051G>T NP_001293061.1:p.Trp1017Cys
NM_002026.2:c.3051G>T NP_002017.1:p.Trp1017Cys
NM_212474.1:c.3051G>T NP_997639.1:p.Trp1017Cys
NM_212476.1:c.3051G>T NP_997641.1:p.Trp1017Cys
NM_212478.1:c.3051G>T NP_997643.1:p.Trp1017Cys
NM_212482.1:c.3051G>T NP_997647.1:p.Trp1017Cys
XM_005246397.1:c.3051G>T XP_005246454.1:p.Trp1017Cys
XM_005246398.1:c.3051G>T XP_005246455.1:p.Trp1017Cys
XM_005246399.1:c.3051G>T XP_005246456.1:p.Trp1017Cys
XM_005246401.1:c.3051G>T XP_005246458.1:p.Trp1017Cys
XM_005246402.1:c.3051G>T XP_005246459.1:p.Trp1017Cys
XM_005246403.1:c.3051G>T XP_005246460.1:p.Trp1017Cys
XM_005246404.1:c.3051G>T XP_005246461.1:p.Trp1017Cys
XM_005246405.1:c.3051G>T XP_005246462.1:p.Trp1017Cys
XM_005246406.1:c.3051G>T XP_005246463.1:p.Trp1017Cys
XM_005246407.1:c.3051G>T XP_005246464.1:p.Trp1017Cys
XM_005246408.1:c.3051G>T XP_005246465.1:p.Trp1017Cys
XM_005246409.1:c.3051G>T XP_005246466.1:p.Trp1017Cys
XM_005246410.1:c.3051G>T XP_005246467.1:p.Trp1017Cys
XM_005246411.1:c.3051G>T XP_005246468.1:p.Trp1017Cys
XM_005246412.1:c.3051G>T XP_005246469.1:p.Trp1017Cys
XM_005246414.1:c.3051G>T XP_005246471.1:p.Trp1017Cys
XM_005246416.1:c.3051G>T XP_005246473.1:p.Trp1017Cys
NM_001365517.1:c.3051G>T NP_001352446.1:p.Trp1017Cys
NM_001365518.1:c.3051G>T NP_001352447.1:p.Trp1017Cys
NM_001365519.1:c.3051G>T NP_001352448.1:p.Trp1017Cys
NM_001365520.1:c.3051G>T NP_001352449.1:p.Trp1017Cys
NM_001365521.1:c.3051G>T NP_001352450.1:p.Trp1017Cys
NM_001365522.1:c.3051G>T NP_001352451.1:p.Trp1017Cys
NM_001365523.1:c.3051G>T NP_001352452.1:p.Trp1017Cys
NM_001365524.1:c.3051G>T NP_001352453.1:p.Trp1017Cys
NM_002026.3:c.3051G>T NP_002017.1:p.Trp1017Cys
NM_212474.2:c.3051G>T NP_997639.1:p.Trp1017Cys
NM_212476.2:c.3051G>T NP_997641.1:p.Trp1017Cys
NM_212478.2:c.3051G>T NP_997643.1:p.Trp1017Cys
NM_212482.2:c.3051G>T NP_997647.1:p.Trp1017Cys
XM_017003692.1:c.3051G>T XP_016859181.1:p.Trp1017Cys
XM_017003695.1:c.3051G>T XP_016859184.1:p.Trp1017Cys
XM_024452769.1:c.3051G>T XP_024308537.1:p.Trp1017Cys
XM_024452770.1:c.3051G>T XP_024308538.1:p.Trp1017Cys
NM_212482.3:c.3051G>T NP_997647.1:p.Trp1017Cys
NM_001306129.2:c.3051G>T NP_001293058.2:p.Trp1017Cys
NM_001306130.2:c.3051G>T NP_001293059.2:p.Trp1017Cys
NM_001306131.2:c.3051G>T NP_001293060.2:p.Trp1017Cys
NM_001306132.2:c.3051G>T NP_001293061.2:p.Trp1017Cys
NM_001365517.2:c.3051G>T NP_001352446.1:p.Trp1017Cys
NM_001365518.2:c.3051G>T NP_001352447.1:p.Trp1017Cys
NM_001365519.2:c.3051G>T NP_001352448.1:p.Trp1017Cys
NM_001365520.2:c.3051G>T NP_001352449.1:p.Trp1017Cys
NM_001365521.2:c.3051G>T NP_001352450.1:p.Trp1017Cys
NM_001365522.2:c.3051G>T NP_001352451.1:p.Trp1017Cys
NM_001365523.2:c.3051G>T NP_001352452.1:p.Trp1017Cys
NM_001365524.2:c.3051G>T NP_001352453.1:p.Trp1017Cys
NM_002026.4:c.3051G>T NP_002017.2:p.Trp1017Cys
NM_212474.3:c.3051G>T NP_997639.2:p.Trp1017Cys
NM_212476.3:c.3051G>T NP_997641.2:p.Trp1017Cys
NM_212478.3:c.3051G>T NP_997643.2:p.Trp1017Cys
NM_212482.4:c.3051G>T MANE Select NP_997647.2:p.Trp1017Cys
Search 100 bp 5'
Search 100 bp 3'