Canonical Allele Identifier: CA1742563860

Gene: FLNC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128849256_128849257delinsAG , CM000669.2:g.128849256_128849257delinsAG	GRCh38
NC_000007.13:g.128489310_128489311delinsAG , CM000669.1:g.128489310_128489311delinsAG	GRCh37
NC_000007.12:g.128276546_128276547delinsAG	NCBI36
NG_011807.1:g.23828_23829delinsAG , LRG_870:g.23828_23829delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.4951+52_4951+53delinsAG MANE Select	ENSP00000327145.8:n.4951+52_4951+53delinsAG
ENST00000325888.12:c.4951+52_4951+53delinsAG	ENSP00000327145.8:n.4951+52_4951+53delinsAG
ENST00000346177.6:c.4951+52_4951+53delinsAG	ENSP00000344002.6:n.4951+52_4951+53delinsAG
NM_001127487.1:c.4951+52_4951+53delinsAG	NP_001120959.1:n.4951+52_4951+53delinsAG
NM_001458.4:c.4951+52_4951+53delinsAG , LRG_870t1:c.4951+52_4951+53delinsAG	NP_001449.3:n.4951+52_4951+53delinsAG
NM_001127487.2:c.4951+52_4951+53delinsAG	NP_001120959.1:n.4951+52_4951+53delinsAG
NM_001458.5:c.4951+52_4951+53delinsAG MANE Select	NP_001449.3:n.4951+52_4951+53delinsAG