Canonical Allele Identifier: CA1742520728
Gene: FLNC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128837393C= , CM000669.2:g.128837393C= GRCh38
NC_000007.13:g.128477447C= , CM000669.1:g.128477447C= GRCh37
NC_000007.12:g.128264683C= NCBI36
NG_011807.1:g.11965C= , LRG_870:g.11965C=

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.700-5C= MANE Select ENSP00000327145.8:n.700-5C=
ENST00000325888.12:c.700-5C= ENSP00000327145.8:n.700-5C=
ENST00000346177.6:c.700-5C= ENSP00000344002.6:n.700-5C=
NM_001127487.1:c.700-5C= NP_001120959.1:n.700-5C=
NM_001458.4:c.700-5C= , LRG_870t1:c.700-5C= NP_001449.3:n.700-5C=
NM_001127487.2:c.700-5C= NP_001120959.1:n.700-5C=
NM_001458.5:c.700-5C= MANE Select NP_001449.3:n.700-5C=