Canonical Allele Identifier: CA2579013858
Gene: FLNC HGNC NCBI

Linked Data

gnomAD v4: 7-128837625-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128837625C>T , CM000669.2:g.128837625C>T GRCh38
NC_000007.13:g.128477679C>T , CM000669.1:g.128477679C>T GRCh37
NC_000007.12:g.128264915C>T NCBI36
NG_011807.1:g.12197C>T , LRG_870:g.12197C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.851-12C>T MANE Select ENSP00000327145.8:n.851-12C>T
ENST00000325888.12:c.851-12C>T ENSP00000327145.8:n.851-12C>T
ENST00000346177.6:c.851-12C>T ENSP00000344002.6:n.851-12C>T
NM_001127487.1:c.851-12C>T NP_001120959.1:n.851-12C>T
NM_001458.4:c.851-12C>T , LRG_870t1:c.851-12C>T NP_001449.3:n.851-12C>T
NM_001127487.2:c.851-12C>T NP_001120959.1:n.851-12C>T
NM_001458.5:c.851-12C>T MANE Select NP_001449.3:n.851-12C>T
Search 100 bp 5'
Search 100 bp 3'