Canonical Allele Identifier: CA1742517053
Gene: FLNC HGNC NCBI

Linked Data

dbSNP Id: rs1808046222

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128835161T>G , CM000669.2:g.128835161T>G GRCh38
NC_000007.13:g.128475215T>G , CM000669.1:g.128475215T>G GRCh37
NC_000007.12:g.128262451T>G NCBI36
NG_011807.1:g.9733T>G , LRG_870:g.9733T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.353-165T>G MANE Select ENSP00000327145.8:n.353-165T>G
ENST00000325888.12:c.353-165T>G ENSP00000327145.8:n.353-165T>G
ENST00000346177.6:c.353-165T>G ENSP00000344002.6:n.353-165T>G
NM_001127487.1:c.353-165T>G NP_001120959.1:n.353-165T>G
NM_001458.4:c.353-165T>G , LRG_870t1:c.353-165T>G NP_001449.3:n.353-165T>G
NM_001127487.2:c.353-165T>G NP_001120959.1:n.353-165T>G
NM_001458.5:c.353-165T>G MANE Select NP_001449.3:n.353-165T>G