Canonical Allele Identifier: CA1742579946

Gene: FLNC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128843280_128843282delinsAGC , CM000669.2:g.128843280_128843282delinsAGC	GRCh38
NC_000007.13:g.128483334_128483336delinsAGC , CM000669.1:g.128483334_128483336delinsAGC	GRCh37
NC_000007.12:g.128270570_128270572delinsAGC	NCBI36
NG_011807.1:g.17852_17854delinsAGC , LRG_870:g.17852_17854delinsAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.2602_2604delinsAGC MANE Select	ENSP00000327145.8:p.Ser868=
ENST00000325888.12:c.2602_2604delinsAGC	ENSP00000327145.8:p.Ser868=
ENST00000346177.6:c.2602_2604delinsAGC	ENSP00000344002.6:p.Ser868=
NM_001127487.1:c.2602_2604delinsAGC	NP_001120959.1:p.Ser868=
NM_001458.4:c.2602_2604delinsAGC , LRG_870t1:c.2602_2604delinsAGC	NP_001449.3:p.Ser868=
NM_001127487.2:c.2602_2604delinsAGC	NP_001120959.1:p.Ser868=
NM_001458.5:c.2602_2604delinsAGC MANE Select	NP_001449.3:p.Ser868=