Canonical Allele Identifier: CA369221817

Gene: FLNC

Linked Data

• MyVariant Identifiers: chr7:g.128477451G>C (hg19) ; chr7:g.128837397G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128837397G>C , CM000669.2:g.128837397G>C	GRCh38
NC_000007.13:g.128477451G>C , CM000669.1:g.128477451G>C	GRCh37
NC_000007.12:g.128264687G>C	NCBI36
NG_011807.1:g.11969G>C , LRG_870:g.11969G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000325888.13:c.700-1G>C MANE Select	ENSP00000327145.8:n.700-1G>C
ENST00000325888.12:c.700-1G>C	ENSP00000327145.8:n.700-1G>C
ENST00000346177.6:c.700-1G>C	ENSP00000344002.6:n.700-1G>C
NM_001127487.1:c.700-1G>C	NP_001120959.1:n.700-1G>C
NM_001458.4:c.700-1G>C , LRG_870t1:c.700-1G>C	NP_001449.3:n.700-1G>C
NM_001127487.2:c.700-1G>C	NP_001120959.1:n.700-1G>C
NM_001458.5:c.700-1G>C MANE Select	NP_001449.3:n.700-1G>C