Canonical Allele Identifier: CA1742566322

Gene: FLNC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128840950G= , CM000669.2:g.128840950G=	GRCh38
NC_000007.13:g.128481004G= , CM000669.1:g.128481004G=	GRCh37
NC_000007.12:g.128268240G=	NCBI36
NG_011807.1:g.15522G= , LRG_870:g.15522G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.1793G= MANE Select	ENSP00000327145.8:p.Gly598=
ENST00000325888.12:c.1793G=	ENSP00000327145.8:p.Gly598=
ENST00000346177.6:c.1793G=	ENSP00000344002.6:p.Gly598=
NM_001127487.1:c.1793G=	NP_001120959.1:p.Gly598=
NM_001458.4:c.1793G= , LRG_870t1:c.1793G=	NP_001449.3:p.Gly598=
NM_001127487.2:c.1793G=	NP_001120959.1:p.Gly598=
NM_001458.5:c.1793G= MANE Select	NP_001449.3:p.Gly598=