Canonical Allele Identifier: CA1742563569

Gene: FLNC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128849138_128849144delinsCACGTTG , CM000669.2:g.128849138_128849144delinsCACGTTG	GRCh38
NC_000007.13:g.128489192_128489198delinsCACGTTG , CM000669.1:g.128489192_128489198delinsCACGTTG	GRCh37
NC_000007.12:g.128276428_128276434delinsCACGTTG	NCBI36
NG_011807.1:g.23710_23716delinsCACGTTG , LRG_870:g.23710_23716delinsCACGTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.4928-43_4928-37delinsCACGTTG MANE Select	ENSP00000327145.8:n.4928-43_4928-37delinsCACGTTG
ENST00000325888.12:c.4928-43_4928-37delinsCACGTTG	ENSP00000327145.8:n.4928-43_4928-37delinsCACGTTG
ENST00000346177.6:c.4928-43_4928-37delinsCACGTTG	ENSP00000344002.6:n.4928-43_4928-37delinsCACGTTG
NM_001127487.1:c.4928-43_4928-37delinsCACGTTG	NP_001120959.1:n.4928-43_4928-37delinsCACGTTG
NM_001458.4:c.4928-43_4928-37delinsCACGTTG , LRG_870t1:c.4928-43_4928-37delinsCACGTTG	NP_001449.3:n.4928-43_4928-37delinsCACGTTG
NM_001127487.2:c.4928-43_4928-37delinsCACGTTG	NP_001120959.1:n.4928-43_4928-37delinsCACGTTG
NM_001458.5:c.4928-43_4928-37delinsCACGTTG MANE Select	NP_001449.3:n.4928-43_4928-37delinsCACGTTG