Canonical Allele Identifier: CA1742565084
Gene: FLNC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128849586C= , CM000669.2:g.128849586C= GRCh38
NC_000007.13:g.128489640C= , CM000669.1:g.128489640C= GRCh37
NC_000007.12:g.128276876C= NCBI36
NG_011807.1:g.24158C= , LRG_870:g.24158C=

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.5199+8C= MANE Select ENSP00000327145.8:n.5199+8C=
ENST00000325888.12:c.5199+8C= ENSP00000327145.8:n.5199+8C=
ENST00000346177.6:c.5199+8C= ENSP00000344002.6:n.5199+8C=
NM_001127487.1:c.5199+8C= NP_001120959.1:n.5199+8C=
NM_001458.4:c.5199+8C= , LRG_870t1:c.5199+8C= NP_001449.3:n.5199+8C=
NM_001127487.2:c.5199+8C= NP_001120959.1:n.5199+8C=
NM_001458.5:c.5199+8C= MANE Select NP_001449.3:n.5199+8C=
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