Canonical Allele Identifier: CA369202038
Gene: FLNC HGNC NCBI

Linked Data

dbSNP Id: rs1358403336
gnomAD v4: 7-128848058-G-T
MyVariant Identifiers: chr7:g.128488112G>T (hg19) chr7:g.128848058G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128848058G>T , CM000669.2:g.128848058G>T GRCh38
NC_000007.13:g.128488112G>T , CM000669.1:g.128488112G>T GRCh37
NC_000007.12:g.128275348G>T NCBI36
NG_011807.1:g.22630G>T , LRG_870:g.22630G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.4570G>T MANE Select ENSP00000327145.8:p.Val1524Leu
ENST00000325888.12:c.4570G>T ENSP00000327145.8:p.Val1524Leu
ENST00000346177.6:c.4570G>T ENSP00000344002.6:p.Val1524Leu
NM_001127487.1:c.4570G>T NP_001120959.1:p.Val1524Leu
NM_001458.4:c.4570G>T , LRG_870t1:c.4570G>T NP_001449.3:p.Val1524Leu
NM_001127487.2:c.4570G>T NP_001120959.1:p.Val1524Leu
NM_001458.5:c.4570G>T MANE Select NP_001449.3:p.Val1524Leu
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