Canonical Allele Identifier: CA1742580890

Gene: FLNC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128843543_128843546delinsACTC , CM000669.2:g.128843543_128843546delinsACTC	GRCh38
NC_000007.13:g.128483597_128483600delinsACTC , CM000669.1:g.128483597_128483600delinsACTC	GRCh37
NC_000007.12:g.128270833_128270836delinsACTC	NCBI36
NG_011807.1:g.18115_18118delinsACTC , LRG_870:g.18115_18118delinsACTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.2777_2780delinsACTC MANE Select	ENSP00000327145.8:p.Tyr926=
ENST00000325888.12:c.2777_2780delinsACTC	ENSP00000327145.8:p.Tyr926=
ENST00000346177.6:c.2777_2780delinsACTC	ENSP00000344002.6:p.Tyr926=
NM_001127487.1:c.2777_2780delinsACTC	NP_001120959.1:p.Tyr926=
NM_001458.4:c.2777_2780delinsACTC , LRG_870t1:c.2777_2780delinsACTC	NP_001449.3:p.Tyr926=
NM_001127487.2:c.2777_2780delinsACTC	NP_001120959.1:p.Tyr926=
NM_001458.5:c.2777_2780delinsACTC MANE Select	NP_001449.3:p.Tyr926=