Canonical Allele Identifier: CA1742588464
Gene: FLNC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128846788T= , CM000669.2:g.128846788T= GRCh38
NC_000007.13:g.128486842T= , CM000669.1:g.128486842T= GRCh37
NC_000007.12:g.128274078T= NCBI36
NG_011807.1:g.21360T= , LRG_870:g.21360T=

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.4171T= MANE Select ENSP00000327145.8:p.Ser1391=
ENST00000325888.12:c.4171T= ENSP00000327145.8:p.Ser1391=
ENST00000346177.6:c.4171T= ENSP00000344002.6:p.Ser1391=
NM_001127487.1:c.4171T= NP_001120959.1:p.Ser1391=
NM_001458.4:c.4171T= , LRG_870t1:c.4171T= NP_001449.3:p.Ser1391=
NM_001127487.2:c.4171T= NP_001120959.1:p.Ser1391=
NM_001458.5:c.4171T= MANE Select NP_001449.3:p.Ser1391=
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