Canonical Allele Identifier: CA2842613792

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154371162_154371163insGTATCATTA , CM000685.2:g.154371162_154371163insGTATCATTA	GRCh38
NC_000023.10:g.153599530_153599531insGTATCATTA , CM000685.1:g.153599530_153599531insGTATCATTA	GRCh37
NC_000023.9:g.153252724_153252725insGTATCATTA	NCBI36
NG_008677.1:g.1735_1736insGTATCATTA , LRG_745:g.1735_1736insGTATCATTA
NG_011506.1:g.8476_8477insTAATGATAC
NG_011506.2:g.8476_8477insTAATGATAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.83_84insTAATGATAC	ENSP00000353467.4:p.Met28delinsIleAsnAspThr
ENST00000369850.10:c.83_84insTAATGATAC MANE Select	ENSP00000358866.3:p.Met28delinsIleAsnAspThr
ENST00000369856.8:c.2_3insTAATGATAC	ENSP00000358872.4:p.Met1delinsIleAsnAspThr
ENST00000422373.6:c.83_84insTAATGATAC	ENSP00000416926.2:p.Met28delinsIleAsnAspThr
ENST00000610817.5:c.83_84insTAATGATAC	ENSP00000480593.2:p.Met28delinsIleAsnAspThr
ENST00000676696.1:c.83_84insTAATGATAC	ENSP00000503392.1:p.Met28delinsIleAsnAspThr
ENST00000344736.8:c.83_84insTAATGATAC	ENSP00000358863.3:p.Met28delinsIleAsnAspThr
ENST00000360319.8:c.83_84insTAATGATAC	ENSP00000353467.4:p.Met28delinsIleAsnAspThr
ENST00000369850.7:c.83_84insTAATGATAC	ENSP00000358866.3:p.Met28delinsIleAsnAspThr
ENST00000369856.7:c.2_3insTAATGATAC	ENSP00000358872.4:p.Met1delinsIleAsnAspThr
ENST00000420627.5:c.41_42insTAATGATAC	ENSP00000408921.1:p.Met14delinsIleAsnAspThr
ENST00000422373.5:c.83_84insTAATGATAC	ENSP00000416926.1:p.Met28delinsIleAsnAspThr
ENST00000610817.4:c.2_3insTAATGATAC	ENSP00000480593.1:p.Met1delinsIleAsnAspThr
NM_001110556.1:c.83_84insTAATGATAC	NP_001104026.1:p.Met28delinsIleAsnAspThr
NM_001456.3:c.83_84insTAATGATAC	NP_001447.2:p.Met28delinsIleAsnAspThr
XM_011531127.1:c.83_84insTAATGATAC	XP_011529429.1:p.Met28delinsIleAsnAspThr
XM_011531128.1:c.83_84insTAATGATAC	XP_011529430.1:p.Met28delinsIleAsnAspThr
XM_011531129.1:c.83_84insTAATGATAC	XP_011529431.1:p.Met28delinsIleAsnAspThr
XM_011531130.1:c.83_84insTAATGATAC	XP_011529432.1:p.Met28delinsIleAsnAspThr
XM_011531131.1:c.83_84insTAATGATAC	XP_011529433.1:p.Met28delinsIleAsnAspThr
NM_001110556.2:c.83_84insTAATGATAC MANE Select	NP_001104026.1:p.Met28delinsIleAsnAspThr
NM_001456.4:c.83_84insTAATGATAC	NP_001447.2:p.Met28delinsIleAsnAspThr