Canonical Allele Identifier: CA1742589538

Gene: FLNC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128848024C= , CM000669.2:g.128848024C=	GRCh38
NC_000007.13:g.128488078C= , CM000669.1:g.128488078C=	GRCh37
NC_000007.12:g.128275314C=	NCBI36
NG_011807.1:g.22596C= , LRG_870:g.22596C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.4536C= MANE Select	ENSP00000327145.8:p.Pro1512=
ENST00000325888.12:c.4536C=	ENSP00000327145.8:p.Pro1512=
ENST00000346177.6:c.4536C=	ENSP00000344002.6:p.Pro1512=
NM_001127487.1:c.4536C=	NP_001120959.1:p.Pro1512=
NM_001458.4:c.4536C= , LRG_870t1:c.4536C=	NP_001449.3:p.Pro1512=
NM_001127487.2:c.4536C=	NP_001120959.1:p.Pro1512=
NM_001458.5:c.4536C= MANE Select	NP_001449.3:p.Pro1512=