Canonical Allele Identifier: CA2695219218
Gene: CFL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.34713429_34713430del , CM000676.2:g.34713429_34713430del GRCh38
NC_000014.8:g.35182635_35182636del , CM000676.1:g.35182635_35182636del GRCh37
NC_000014.7:g.34252386_34252387del NCBI36
NG_012740.1:g.6395_6396del , LRG_213:g.6395_6396del

Transcript Alleles

HGVS Amino-acid Change
ENST00000298159.11:c.136_137del MANE Select ENSP00000298159.6:p.Gln46AsnfsTer13
ENST00000341223.8:c.136_137del ENSP00000340635.3:p.Gln46AsnfsTer13
ENST00000672163.1:c.136_137del ENSP00000500375.1:p.Gln46AsnfsTer13
ENST00000672517.1:c.136_137del ENSP00000500532.1:p.Gln46AsnfsTer13
ENST00000673315.1:c.85_86del ENSP00000500002.1:p.Gln29AsnfsTer13
ENST00000298159.10:c.136_137del ENSP00000298159.6:p.Gln46AsnfsTer13
ENST00000341223.7:c.136_137del ENSP00000340635.3:p.Gln46AsnfsTer13
ENST00000422678.2:c.136_137del ENSP00000409326.2:p.Gln46AsnfsTer18
ENST00000554470.5:c.57+79_57+80del ENSP00000450862.1:n.57+79_57+80del
ENST00000555765.5:c.85_86del ENSP00000452451.1:p.Gln29AsnfsTer13
ENST00000556161.1:c.85_86del ENSP00000452188.1:p.Gln29AsnfsTer13
NM_001243645.1:c.85_86del NP_001230574.1:p.Gln29AsnfsTer13
NM_021914.7:c.136_137del NP_068733.1:p.Gln46AsnfsTer13
NM_138638.4:c.136_137del , LRG_213t1:c.136_137del NP_619579.1:p.Gln46AsnfsTer13
NR_028130.1:n.419_420del
NR_028131.1:n.340+79_340+80del
XM_011536363.1:c.85_86del XP_011534665.1:p.Gln29AsnfsTer13
XM_011536363.3:c.85_86del XP_011534665.1:p.Gln29AsnfsTer13
NM_138638.5:c.136_137del MANE Select NP_619579.1:p.Gln46AsnfsTer13
NM_001243645.2:c.85_86del NP_001230574.1:p.Gln29AsnfsTer13
NM_021914.8:c.136_137del NP_068733.1:p.Gln46AsnfsTer13
NR_028130.2:n.189_190del
NR_028131.2:n.110+79_110+80del