Canonical Allele Identifier: CA1742565068

Gene: FLNC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128849580T= , CM000669.2:g.128849580T=	GRCh38
NC_000007.13:g.128489634T= , CM000669.1:g.128489634T=	GRCh37
NC_000007.12:g.128276870T=	NCBI36
NG_011807.1:g.24152T= , LRG_870:g.24152T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000325888.13:c.5199+2T= MANE Select	ENSP00000327145.8:n.5199+2T=
ENST00000325888.12:c.5199+2T=	ENSP00000327145.8:n.5199+2T=
ENST00000346177.6:c.5199+2T=	ENSP00000344002.6:n.5199+2T=
NM_001127487.1:c.5199+2T=	NP_001120959.1:n.5199+2T=
NM_001458.4:c.5199+2T= , LRG_870t1:c.5199+2T=	NP_001449.3:n.5199+2T=
NM_001127487.2:c.5199+2T=	NP_001120959.1:n.5199+2T=
NM_001458.5:c.5199+2T= MANE Select	NP_001449.3:n.5199+2T=