Canonical Allele Identifier: CA2579014170

Gene: FLNC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128843727A>T , CM000669.2:g.128843727A>T	GRCh38
NC_000007.13:g.128483781A>T , CM000669.1:g.128483781A>T	GRCh37
NC_000007.12:g.128271017A>T	NCBI36
NG_011807.1:g.18299A>T , LRG_870:g.18299A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.2812-69A>T MANE Select	ENSP00000327145.8:n.2812-69A>T
ENST00000325888.12:c.2812-69A>T	ENSP00000327145.8:n.2812-69A>T
ENST00000346177.6:c.2812-69A>T	ENSP00000344002.6:n.2812-69A>T
NM_001127487.1:c.2812-69A>T	NP_001120959.1:n.2812-69A>T
NM_001458.4:c.2812-69A>T , LRG_870t1:c.2812-69A>T	NP_001449.3:n.2812-69A>T
NM_001127487.2:c.2812-69A>T	NP_001120959.1:n.2812-69A>T
NM_001458.5:c.2812-69A>T MANE Select	NP_001449.3:n.2812-69A>T