Canonical Allele Identifier: CA369191661
Gene: FLNC HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.128482915C>A (hg19) chr7:g.128842861C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128842861C>A , CM000669.2:g.128842861C>A GRCh38
NC_000007.13:g.128482915C>A , CM000669.1:g.128482915C>A GRCh37
NC_000007.12:g.128270151C>A NCBI36
NG_011807.1:g.17433C>A , LRG_870:g.17433C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.2457C>A MANE Select ENSP00000327145.8:p.Phe819Leu
ENST00000325888.12:c.2457C>A ENSP00000327145.8:p.Phe819Leu
ENST00000346177.6:c.2457C>A ENSP00000344002.6:p.Phe819Leu
NM_001127487.1:c.2457C>A NP_001120959.1:p.Phe819Leu
NM_001458.4:c.2457C>A , LRG_870t1:c.2457C>A NP_001449.3:p.Phe819Leu
NM_001127487.2:c.2457C>A NP_001120959.1:p.Phe819Leu
NM_001458.5:c.2457C>A MANE Select NP_001449.3:p.Phe819Leu
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