Canonical Allele Identifier: CA2695208487

Gene: FLNC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128845057dup , CM000669.2:g.128845057dup	GRCh38
NC_000007.13:g.128485111dup , CM000669.1:g.128485111dup	GRCh37
NC_000007.12:g.128272347dup	NCBI36
NG_011807.1:g.19629dup , LRG_870:g.19629dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.3592dup MANE Select	ENSP00000327145.8:p.Val1198GlyfsTer?
ENST00000325888.12:c.3592dup	ENSP00000327145.8:p.Val1198GlyfsTer?
ENST00000346177.6:c.3592dup	ENSP00000344002.6:p.Val1198GlyfsTer?
NM_001127487.1:c.3592dup	NP_001120959.1:p.Val1198GlyfsTer?
NM_001458.4:c.3592dup , LRG_870t1:c.3592dup	NP_001449.3:p.Val1198GlyfsTer?
NM_001127487.2:c.3592dup	NP_001120959.1:p.Val1198GlyfsTer?
NM_001458.5:c.3592dup MANE Select	NP_001449.3:p.Val1198GlyfsTer?