Canonical Allele Identifier: CA2684815661
Gene: FLNC HGNC NCBI

Linked Data

gnomAD v4: 7-128843219-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128843219C>A , CM000669.2:g.128843219C>A GRCh38
NC_000007.13:g.128483273C>A , CM000669.1:g.128483273C>A GRCh37
NC_000007.12:g.128270509C>A NCBI36
NG_011807.1:g.17791C>A , LRG_870:g.17791C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.2551-10C>A MANE Select ENSP00000327145.8:n.2551-10C>A
ENST00000325888.12:c.2551-10C>A ENSP00000327145.8:n.2551-10C>A
ENST00000346177.6:c.2551-10C>A ENSP00000344002.6:n.2551-10C>A
NM_001127487.1:c.2551-10C>A NP_001120959.1:n.2551-10C>A
NM_001458.4:c.2551-10C>A , LRG_870t1:c.2551-10C>A NP_001449.3:n.2551-10C>A
NM_001127487.2:c.2551-10C>A NP_001120959.1:n.2551-10C>A
NM_001458.5:c.2551-10C>A MANE Select NP_001449.3:n.2551-10C>A
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