Canonical Allele Identifier: CA1742589483

Gene: FLNC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128847992A= , CM000669.2:g.128847992A=	GRCh38
NC_000007.13:g.128488046A= , CM000669.1:g.128488046A=	GRCh37
NC_000007.12:g.128275282A=	NCBI36
NG_011807.1:g.22564A= , LRG_870:g.22564A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.4504A= MANE Select	ENSP00000327145.8:p.Thr1502=
ENST00000325888.12:c.4504A=	ENSP00000327145.8:p.Thr1502=
ENST00000346177.6:c.4504A=	ENSP00000344002.6:p.Thr1502=
NM_001127487.1:c.4504A=	NP_001120959.1:p.Thr1502=
NM_001458.4:c.4504A= , LRG_870t1:c.4504A=	NP_001449.3:p.Thr1502=
NM_001127487.2:c.4504A=	NP_001120959.1:p.Thr1502=
NM_001458.5:c.4504A= MANE Select	NP_001449.3:p.Thr1502=