Canonical Allele Identifier: CA1742563952
Gene: FLNC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128849302C= , CM000669.2:g.128849302C= GRCh38
NC_000007.13:g.128489356C= , CM000669.1:g.128489356C= GRCh37
NC_000007.12:g.128276592C= NCBI36
NG_011807.1:g.23874C= , LRG_870:g.23874C=

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.4952-29C= MANE Select ENSP00000327145.8:n.4952-29C=
ENST00000325888.12:c.4952-29C= ENSP00000327145.8:n.4952-29C=
ENST00000346177.6:c.4952-29C= ENSP00000344002.6:n.4952-29C=
NM_001127487.1:c.4952-29C= NP_001120959.1:n.4952-29C=
NM_001458.4:c.4952-29C= , LRG_870t1:c.4952-29C= NP_001449.3:n.4952-29C=
NM_001127487.2:c.4952-29C= NP_001120959.1:n.4952-29C=
NM_001458.5:c.4952-29C= MANE Select NP_001449.3:n.4952-29C=
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