Canonical Allele Identifier: CA369222526
Gene: FLNC HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.128477555T>C (hg19) chr7:g.128837501T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128837501T>C , CM000669.2:g.128837501T>C GRCh38
NC_000007.13:g.128477555T>C , CM000669.1:g.128477555T>C GRCh37
NC_000007.12:g.128264791T>C NCBI36
NG_011807.1:g.12073T>C , LRG_870:g.12073T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.803T>C MANE Select ENSP00000327145.8:p.Val268Ala
ENST00000325888.12:c.803T>C ENSP00000327145.8:p.Val268Ala
ENST00000346177.6:c.803T>C ENSP00000344002.6:p.Val268Ala
NM_001127487.1:c.803T>C NP_001120959.1:p.Val268Ala
NM_001458.4:c.803T>C , LRG_870t1:c.803T>C NP_001449.3:p.Val268Ala
NM_001127487.2:c.803T>C NP_001120959.1:p.Val268Ala
NM_001458.5:c.803T>C MANE Select NP_001449.3:p.Val268Ala
Search 100 bp 5'
Search 100 bp 3'