Canonical Allele Identifier: CA1742563656

Gene: FLNC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128849167_128849169delinsTTC , CM000669.2:g.128849167_128849169delinsTTC	GRCh38
NC_000007.13:g.128489221_128489223delinsTTC , CM000669.1:g.128489221_128489223delinsTTC	GRCh37
NC_000007.12:g.128276457_128276459delinsTTC	NCBI36
NG_011807.1:g.23739_23741delinsTTC , LRG_870:g.23739_23741delinsTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.4928-14_4928-12delinsTTC MANE Select	ENSP00000327145.8:n.4928-14_4928-12delinsTTC
ENST00000325888.12:c.4928-14_4928-12delinsTTC	ENSP00000327145.8:n.4928-14_4928-12delinsTTC
ENST00000346177.6:c.4928-14_4928-12delinsTTC	ENSP00000344002.6:n.4928-14_4928-12delinsTTC
NM_001127487.1:c.4928-14_4928-12delinsTTC	NP_001120959.1:n.4928-14_4928-12delinsTTC
NM_001458.4:c.4928-14_4928-12delinsTTC , LRG_870t1:c.4928-14_4928-12delinsTTC	NP_001449.3:n.4928-14_4928-12delinsTTC
NM_001127487.2:c.4928-14_4928-12delinsTTC	NP_001120959.1:n.4928-14_4928-12delinsTTC
NM_001458.5:c.4928-14_4928-12delinsTTC MANE Select	NP_001449.3:n.4928-14_4928-12delinsTTC