Canonical Allele Identifier: CA2538121303

Gene: FLNC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128849243_128849244insCGGTGCTCAAC , CM000669.2:g.128849243_128849244insCGGTGCTCAAC	GRCh38
NC_000007.13:g.128489297_128489298insCGGTGCTCAAC , CM000669.1:g.128489297_128489298insCGGTGCTCAAC	GRCh37
NC_000007.12:g.128276533_128276534insCGGTGCTCAAC	NCBI36
NG_011807.1:g.23815_23816insCGGTGCTCAAC , LRG_870:g.23815_23816insCGGTGCTCAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.4951+39_4951+40insCGGTGCTCAAC MANE Select	ENSP00000327145.8:n.4951+39_4951+40insCGGTGCTCAAC
ENST00000325888.12:c.4951+39_4951+40insCGGTGCTCAAC	ENSP00000327145.8:n.4951+39_4951+40insCGGTGCTCAAC
ENST00000346177.6:c.4951+39_4951+40insCGGTGCTCAAC	ENSP00000344002.6:n.4951+39_4951+40insCGGTGCTCAAC
NM_001127487.1:c.4951+39_4951+40insCGGTGCTCAAC	NP_001120959.1:n.4951+39_4951+40insCGGTGCTCAAC
NM_001458.4:c.4951+39_4951+40insCGGTGCTCAAC , LRG_870t1:c.4951+39_4951+40insCGGTGCTCAAC	NP_001449.3:n.4951+39_4951+40insCGGTGCTCAAC
NM_001127487.2:c.4951+39_4951+40insCGGTGCTCAAC	NP_001120959.1:n.4951+39_4951+40insCGGTGCTCAAC
NM_001458.5:c.4951+39_4951+40insCGGTGCTCAAC MANE Select	NP_001449.3:n.4951+39_4951+40insCGGTGCTCAAC