Canonical Allele Identifier: CA2695208482

Gene: FLNC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128843557_128843571del , CM000669.2:g.128843557_128843571del	GRCh38
NC_000007.13:g.128483611_128483625del , CM000669.1:g.128483611_128483625del	GRCh37
NC_000007.12:g.128270847_128270861del	NCBI36
NG_011807.1:g.18129_18143del , LRG_870:g.18129_18143del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.2791_2805del MANE Select	ENSP00000327145.8:p.Lys931_Val935del
ENST00000325888.12:c.2791_2805del	ENSP00000327145.8:p.Lys931_Val935del
ENST00000346177.6:c.2791_2805del	ENSP00000344002.6:p.Lys931_Val935del
NM_001127487.1:c.2791_2805del	NP_001120959.1:p.Lys931_Val935del
NM_001458.4:c.2791_2805del , LRG_870t1:c.2791_2805del	NP_001449.3:p.Lys931_Val935del
NM_001127487.2:c.2791_2805del	NP_001120959.1:p.Lys931_Val935del
NM_001458.5:c.2791_2805del MANE Select	NP_001449.3:p.Lys931_Val935del