Canonical Allele Identifier: CA2503930869

Gene: FLNC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128849242_128849243insATCTC , CM000669.2:g.128849242_128849243insATCTC	GRCh38
NC_000007.13:g.128489296_128489297insATCTC , CM000669.1:g.128489296_128489297insATCTC	GRCh37
NC_000007.12:g.128276532_128276533insATCTC	NCBI36
NG_011807.1:g.23814_23815insATCTC , LRG_870:g.23814_23815insATCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.4951+38_4951+39insATCTC MANE Select	ENSP00000327145.8:n.4951+38_4951+39insATCTC
ENST00000325888.12:c.4951+38_4951+39insATCTC	ENSP00000327145.8:n.4951+38_4951+39insATCTC
ENST00000346177.6:c.4951+38_4951+39insATCTC	ENSP00000344002.6:n.4951+38_4951+39insATCTC
NM_001127487.1:c.4951+38_4951+39insATCTC	NP_001120959.1:n.4951+38_4951+39insATCTC
NM_001458.4:c.4951+38_4951+39insATCTC , LRG_870t1:c.4951+38_4951+39insATCTC	NP_001449.3:n.4951+38_4951+39insATCTC
NM_001127487.2:c.4951+38_4951+39insATCTC	NP_001120959.1:n.4951+38_4951+39insATCTC
NM_001458.5:c.4951+38_4951+39insATCTC MANE Select	NP_001449.3:n.4951+38_4951+39insATCTC