Canonical Allele Identifier: CA1742580922

Gene: FLNC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128843553_128843565delinsTGTCAAGTACACC , CM000669.2:g.128843553_128843565delinsTGTCAAGTACACC	GRCh38
NC_000007.13:g.128483607_128483619delinsTGTCAAGTACACC , CM000669.1:g.128483607_128483619delinsTGTCAAGTACACC	GRCh37
NC_000007.12:g.128270843_128270855delinsTGTCAAGTACACC	NCBI36
NG_011807.1:g.18125_18137delinsTGTCAAGTACACC , LRG_870:g.18125_18137delinsTGTCAAGTACACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.2787_2799delinsTGTCAAGTACACC MANE Select	ENSP00000327145.8:p.Thr929=
ENST00000325888.12:c.2787_2799delinsTGTCAAGTACACC	ENSP00000327145.8:p.Thr929=
ENST00000346177.6:c.2787_2799delinsTGTCAAGTACACC	ENSP00000344002.6:p.Thr929=
NM_001127487.1:c.2787_2799delinsTGTCAAGTACACC	NP_001120959.1:p.Thr929=
NM_001458.4:c.2787_2799delinsTGTCAAGTACACC , LRG_870t1:c.2787_2799delinsTGTCAAGTACACC	NP_001449.3:p.Thr929=
NM_001127487.2:c.2787_2799delinsTGTCAAGTACACC	NP_001120959.1:p.Thr929=
NM_001458.5:c.2787_2799delinsTGTCAAGTACACC MANE Select	NP_001449.3:p.Thr929=