Canonical Allele Identifier: CA1742579335
Gene: FLNC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128843166A= , CM000669.2:g.128843166A= GRCh38
NC_000007.13:g.128483220A= , CM000669.1:g.128483220A= GRCh37
NC_000007.12:g.128270456A= NCBI36
NG_011807.1:g.17738A= , LRG_870:g.17738A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.2551-63A= MANE Select ENSP00000327145.8:n.2551-63A=
ENST00000325888.12:c.2551-63A= ENSP00000327145.8:n.2551-63A=
ENST00000346177.6:c.2551-63A= ENSP00000344002.6:n.2551-63A=
NM_001127487.1:c.2551-63A= NP_001120959.1:n.2551-63A=
NM_001458.4:c.2551-63A= , LRG_870t1:c.2551-63A= NP_001449.3:n.2551-63A=
NM_001127487.2:c.2551-63A= NP_001120959.1:n.2551-63A=
NM_001458.5:c.2551-63A= MANE Select NP_001449.3:n.2551-63A=