Canonical Allele Identifier: CA369201865
Gene: FLNC HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.128488028A>T (hg19) chr7:g.128847974A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128847974A>T , CM000669.2:g.128847974A>T GRCh38
NC_000007.13:g.128488028A>T , CM000669.1:g.128488028A>T GRCh37
NC_000007.12:g.128275264A>T NCBI36
NG_011807.1:g.22546A>T , LRG_870:g.22546A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.4486A>T MANE Select ENSP00000327145.8:p.Asn1496Tyr
ENST00000325888.12:c.4486A>T ENSP00000327145.8:p.Asn1496Tyr
ENST00000346177.6:c.4486A>T ENSP00000344002.6:p.Asn1496Tyr
NM_001127487.1:c.4486A>T NP_001120959.1:p.Asn1496Tyr
NM_001458.4:c.4486A>T , LRG_870t1:c.4486A>T NP_001449.3:p.Asn1496Tyr
NM_001127487.2:c.4486A>T NP_001120959.1:p.Asn1496Tyr
NM_001458.5:c.4486A>T MANE Select NP_001449.3:p.Asn1496Tyr
Search 100 bp 5'
Search 100 bp 3'