Canonical Allele Identifier: CA3071257276

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154359988A= , CM000685.2:g.154359988A=	GRCh38
NC_000023.10:g.153588356A= , CM000685.1:g.153588356A=	GRCh37
NC_000023.9:g.153241550A=	NCBI36
NG_011506.1:g.19651T=
NG_011506.2:g.19651T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001110556.2:c.3805+2T= MANE Select	NP_001104026.1:n.3805+2T=
ENST00000369850.10:c.3805+2T= MANE Select	ENSP00000358866.3:n.3805+2T=
NM_001110556.1:c.3805+2T=	NP_001104026.1:n.3805+2T=
NM_001456.3:c.3805+2T=	NP_001447.2:n.3805+2T=
NM_001456.4:c.3805+2T=	NP_001447.2:n.3805+2T=
ENST00000344736.8:c.3805+2T=	ENSP00000358863.3:n.3805+2T=
ENST00000360319.8:c.3805+2T=	ENSP00000353467.4:n.3805+2T=
ENST00000360319.9:c.3805+2T=	ENSP00000353467.4:n.3805+2T=
ENST00000369850.7:c.3805+2T=	ENSP00000358866.3:n.3805+2T=
ENST00000369856.7:c.3724+2T=	ENSP00000358872.4:n.3724+2T=
ENST00000369856.8:c.3724+2T=	ENSP00000358872.4:n.3724+2T=
ENST00000420627.5:c.3761+2T=	ENSP00000408921.1:n.3761+2T=
ENST00000422373.5:c.3805+2T=	ENSP00000416926.1:n.3805+2T=
ENST00000422373.6:c.3160+1367T=	ENSP00000416926.2:n.3160+1367T=
ENST00000610817.4:c.3724+2T=	ENSP00000480593.1:n.3724+2T=
ENST00000610817.5:c.3862+2T=	ENSP00000480593.2:n.3862+2T=
ENST00000673639.2:c.279+5448T=
ENST00000676696.1:c.4084+2T=	ENSP00000503392.1:n.4084+2T=
XM_011531127.1:c.3805+2T=	XP_011529429.1:n.3805+2T=
XM_011531128.1:c.3805+2T=	XP_011529430.1:n.3805+2T=
XM_011531129.1:c.3805+2T=	XP_011529431.1:n.3805+2T=
XM_011531130.1:c.3805+2T=	XP_011529432.1:n.3805+2T=
XM_011531131.1:c.3604+2T=	XP_011529433.1:n.3604+2T=