Canonical Allele Identifier: CA1742520746

Gene: FLNC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128837403T= , CM000669.2:g.128837403T=	GRCh38
NC_000007.13:g.128477457T= , CM000669.1:g.128477457T=	GRCh37
NC_000007.12:g.128264693T=	NCBI36
NG_011807.1:g.11975T= , LRG_870:g.11975T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000325888.13:c.705T= MANE Select	ENSP00000327145.8:p.Ile235=
ENST00000325888.12:c.705T=	ENSP00000327145.8:p.Ile235=
ENST00000346177.6:c.705T=	ENSP00000344002.6:p.Ile235=
NM_001127487.1:c.705T=	NP_001120959.1:p.Ile235=
NM_001458.4:c.705T= , LRG_870t1:c.705T=	NP_001449.3:p.Ile235=
NM_001127487.2:c.705T=	NP_001120959.1:p.Ile235=
NM_001458.5:c.705T= MANE Select	NP_001449.3:p.Ile235=