Canonical Allele Identifier: CA2684820161
Gene: FLNC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128839936G>A , CM000669.2:g.128839936G>A GRCh38
NC_000007.13:g.128479990G>A , CM000669.1:g.128479990G>A GRCh37
NC_000007.12:g.128267226G>A NCBI36
NG_011807.1:g.14508G>A , LRG_870:g.14508G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.1412-87G>A MANE Select ENSP00000327145.8:n.1412-87G>A
ENST00000325888.12:c.1412-87G>A ENSP00000327145.8:n.1412-87G>A
ENST00000346177.6:c.1412-87G>A ENSP00000344002.6:n.1412-87G>A
NM_001127487.1:c.1412-87G>A NP_001120959.1:n.1412-87G>A
NM_001458.4:c.1412-87G>A , LRG_870t1:c.1412-87G>A NP_001449.3:n.1412-87G>A
NM_001127487.2:c.1412-87G>A NP_001120959.1:n.1412-87G>A
NM_001458.5:c.1412-87G>A MANE Select NP_001449.3:n.1412-87G>A