Canonical Allele Identifier: CA457577473
Gene: FLNC HGNC NCBI

Linked Data

dbSNP Id: rs2128935898
MyVariant Identifiers: chr7:g.128483285G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128843231G>A , CM000669.2:g.128843231G>A GRCh38
NC_000007.13:g.128483285G>A , CM000669.1:g.128483285G>A GRCh37
NC_000007.12:g.128270521G>A NCBI36
NG_011807.1:g.17803G>A , LRG_870:g.17803G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.2553G>A MANE Select ENSP00000327145.8:p.Glu851=
ENST00000325888.12:c.2553G>A ENSP00000327145.8:p.Glu851=
ENST00000346177.6:c.2553G>A ENSP00000344002.6:p.Glu851=
NM_001127487.1:c.2553G>A NP_001120959.1:p.Glu851=
NM_001458.4:c.2553G>A , LRG_870t1:c.2553G>A NP_001449.3:p.Glu851=
NM_001127487.2:c.2553G>A NP_001120959.1:p.Glu851=
NM_001458.5:c.2553G>A MANE Select NP_001449.3:p.Glu851=