Canonical Allele Identifier: CA833133564

Gene: FLNC

Linked Data

• dbSNP Id: rs1382352158
• gnomAD v4: 7-128837497-CCT-C
• MyVariant Identifiers: chr7:g.128477552_128477553del (hg19) ; chr7:g.128837498_128837499del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128837498_128837499del , CM000669.2:g.128837498_128837499del	GRCh38
NC_000007.13:g.128477552_128477553del , CM000669.1:g.128477552_128477553del	GRCh37
NC_000007.12:g.128264788_128264789del	NCBI36
NG_011807.1:g.12070_12071del , LRG_870:g.12070_12071del

Transcript Alleles

HGVS	Amino-acid change
ENST00000325888.13:c.800_801del MANE Select	ENSP00000327145.8:p.Pro267ArgfsTer?
ENST00000325888.12:c.800_801del	ENSP00000327145.8:p.Pro267ArgfsTer?
ENST00000346177.6:c.800_801del	ENSP00000344002.6:p.Pro267ArgfsTer?
NM_001127487.1:c.800_801del	NP_001120959.1:p.Pro267ArgfsTer?
NM_001458.4:c.800_801del , LRG_870t1:c.800_801del	NP_001449.3:p.Pro267ArgfsTer?
NM_001127487.2:c.800_801del	NP_001120959.1:p.Pro267ArgfsTer?
NM_001458.5:c.800_801del MANE Select	NP_001449.3:p.Pro267ArgfsTer?