Canonical Allele Identifier: CA1742588486
Gene: FLNC HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128846797A= , CM000669.2:g.128846797A= GRCh38
NC_000007.13:g.128486851A= , CM000669.1:g.128486851A= GRCh37
NC_000007.12:g.128274087A= NCBI36
NG_011807.1:g.21369A= , LRG_870:g.21369A=

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.4180A= MANE Select ENSP00000327145.8:p.Lys1394=
ENST00000325888.12:c.4180A= ENSP00000327145.8:p.Lys1394=
ENST00000346177.6:c.4180A= ENSP00000344002.6:p.Lys1394=
NM_001127487.1:c.4180A= NP_001120959.1:p.Lys1394=
NM_001458.4:c.4180A= , LRG_870t1:c.4180A= NP_001449.3:p.Lys1394=
NM_001127487.2:c.4180A= NP_001120959.1:p.Lys1394=
NM_001458.5:c.4180A= MANE Select NP_001449.3:p.Lys1394=
Search 100 bp 5'
Search 100 bp 3'