Canonical Allele Identifier: CA152874
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 129095
dbSNP Id: rs34422412

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128854456A>G , CM000669.2:g.128854456A>G GRCh38
NC_000007.13:g.128494510A>G , CM000669.1:g.128494510A>G GRCh37
NC_000007.12:g.128281746A>G NCBI36
NG_011807.1:g.29028A>G , LRG_870:g.29028A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.6771A>G MANE Select ENSP00000327145.8:p.Pro2257=
ENST00000325888.12:c.6771A>G ENSP00000327145.8:p.Pro2257=
ENST00000346177.6:c.6672A>G ENSP00000344002.6:p.Pro2224=
NM_001127487.1:c.6672A>G NP_001120959.1:p.Pro2224=
NM_001458.4:c.6771A>G , LRG_870t1:c.6771A>G NP_001449.3:p.Pro2257=
NR_149055.1:n.103-1059T>C
NM_001127487.2:c.6672A>G NP_001120959.1:p.Pro2224=
NM_001458.5:c.6771A>G MANE Select NP_001449.3:p.Pro2257=