Canonical Allele Identifier: CA1742566356

Gene: FLNC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128840959T= , CM000669.2:g.128840959T=	GRCh38
NC_000007.13:g.128481013T= , CM000669.1:g.128481013T=	GRCh37
NC_000007.12:g.128268249T=	NCBI36
NG_011807.1:g.15531T= , LRG_870:g.15531T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.1802T= MANE Select	ENSP00000327145.8:p.Val601=
ENST00000325888.12:c.1802T=	ENSP00000327145.8:p.Val601=
ENST00000346177.6:c.1802T=	ENSP00000344002.6:p.Val601=
NM_001127487.1:c.1802T=	NP_001120959.1:p.Val601=
NM_001458.4:c.1802T= , LRG_870t1:c.1802T=	NP_001449.3:p.Val601=
NM_001127487.2:c.1802T=	NP_001120959.1:p.Val601=
NM_001458.5:c.1802T= MANE Select	NP_001449.3:p.Val601=