Canonical Allele Identifier: CA645603465

Gene: FLNA

Linked Data

• COSMIC: COSM5730958 ; COSM5730959

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154362710_154362718del , CM000685.2:g.154362710_154362718del	GRCh38
NC_000023.10:g.153591078_153591086del , CM000685.1:g.153591078_153591086del	GRCh37
NC_000023.9:g.153244272_153244280del	NCBI36
NG_011506.1:g.16922_16930del
NG_011506.2:g.16922_16930del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.2348_2356del	ENSP00000353467.4:p.Gly783_Lys785del
ENST00000369850.10:c.2348_2356del MANE Select	ENSP00000358866.3:p.Gly783_Lys785del
ENST00000369856.8:c.2267_2275del	ENSP00000358872.4:p.Gly756_Lys758del
ENST00000422373.6:c.2348_2356del	ENSP00000416926.2:p.Gly783_Lys785del
ENST00000610817.5:c.2405_2413del	ENSP00000480593.2:n.2405_2413del
ENST00000673639.2:c.279+2719_279+2727del
ENST00000676696.1:c.2627_2635del	ENSP00000503392.1:n.2627_2635del
ENST00000344736.8:c.2348_2356del	ENSP00000358863.3:p.Gly783_Lys785del
ENST00000360319.8:c.2348_2356del	ENSP00000353467.4:p.Gly783_Lys785del
ENST00000369850.7:c.2348_2356del	ENSP00000358866.3:p.Gly783_Lys785del
ENST00000369856.7:c.2267_2275del	ENSP00000358872.4:p.Gly756_Lys758del
ENST00000420627.5:c.2304_2312del	ENSP00000408921.1:n.2304_2312del
ENST00000422373.5:c.2348_2356del	ENSP00000416926.1:p.Gly783_Lys785del
ENST00000610817.4:c.2267_2275del	ENSP00000480593.1:p.Gly756_Lys758del
NM_001110556.1:c.2348_2356del	NP_001104026.1:p.Gly783_Lys785del
NM_001456.3:c.2348_2356del	NP_001447.2:p.Gly783_Lys785del
XM_011531127.1:c.2348_2356del	XP_011529429.1:p.Gly783_Lys785del
XM_011531128.1:c.2348_2356del	XP_011529430.1:p.Gly783_Lys785del
XM_011531129.1:c.2348_2356del	XP_011529431.1:p.Gly783_Lys785del
XM_011531130.1:c.2348_2356del	XP_011529432.1:p.Gly783_Lys785del
XM_011531131.1:c.2147_2155del	XP_011529433.1:p.Gly716_Lys718del
NM_001110556.2:c.2348_2356del MANE Select	NP_001104026.1:p.Gly783_Lys785del
NM_001456.4:c.2348_2356del	NP_001447.2:p.Gly783_Lys785del