Canonical Allele Identifier: CA1742563829

Gene: FLNC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128849252_128849253delinsCG , CM000669.2:g.128849252_128849253delinsCG	GRCh38
NC_000007.13:g.128489306_128489307delinsCG , CM000669.1:g.128489306_128489307delinsCG	GRCh37
NC_000007.12:g.128276542_128276543delinsCG	NCBI36
NG_011807.1:g.23824_23825delinsCG , LRG_870:g.23824_23825delinsCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000325888.13:c.4951+48_4951+49delinsCG MANE Select	ENSP00000327145.8:n.4951+48_4951+49delinsCG
ENST00000325888.12:c.4951+48_4951+49delinsCG	ENSP00000327145.8:n.4951+48_4951+49delinsCG
ENST00000346177.6:c.4951+48_4951+49delinsCG	ENSP00000344002.6:n.4951+48_4951+49delinsCG
NM_001127487.1:c.4951+48_4951+49delinsCG	NP_001120959.1:n.4951+48_4951+49delinsCG
NM_001458.4:c.4951+48_4951+49delinsCG , LRG_870t1:c.4951+48_4951+49delinsCG	NP_001449.3:n.4951+48_4951+49delinsCG
NM_001127487.2:c.4951+48_4951+49delinsCG	NP_001120959.1:n.4951+48_4951+49delinsCG
NM_001458.5:c.4951+48_4951+49delinsCG MANE Select	NP_001449.3:n.4951+48_4951+49delinsCG