Canonical Allele Identifier: CA1742578698
Gene: FLNC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128842990C= , CM000669.2:g.128842990C= GRCh38
NC_000007.13:g.128483044C= , CM000669.1:g.128483044C= GRCh37
NC_000007.12:g.128270280C= NCBI36
NG_011807.1:g.17562C= , LRG_870:g.17562C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.2550+36C= MANE Select ENSP00000327145.8:n.2550+36C=
ENST00000325888.12:c.2550+36C= ENSP00000327145.8:n.2550+36C=
ENST00000346177.6:c.2550+36C= ENSP00000344002.6:n.2550+36C=
NM_001127487.1:c.2550+36C= NP_001120959.1:n.2550+36C=
NM_001458.4:c.2550+36C= , LRG_870t1:c.2550+36C= NP_001449.3:n.2550+36C=
NM_001127487.2:c.2550+36C= NP_001120959.1:n.2550+36C=
NM_001458.5:c.2550+36C= MANE Select NP_001449.3:n.2550+36C=
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