Canonical Allele Identifier: CA2128728631
Gene: CFL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.34713335A= , CM000676.2:g.34713335A= GRCh38
NC_000014.8:g.35182541A= , CM000676.1:g.35182541A= GRCh37
NC_000014.7:g.34252292A= NCBI36
NG_012740.1:g.6489T= , LRG_213:g.6489T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000298159.11:c.230T= MANE Select ENSP00000298159.6:p.Leu77=
ENST00000341223.8:c.230T= ENSP00000340635.3:p.Leu77=
ENST00000672163.1:c.230T= ENSP00000500375.1:p.Leu77=
ENST00000672517.1:c.230T= ENSP00000500532.1:p.Leu77=
ENST00000673315.1:c.179T= ENSP00000500002.1:p.Leu60=
ENST00000298159.10:c.230T= ENSP00000298159.6:p.Leu77=
ENST00000341223.7:c.230T= ENSP00000340635.3:p.Leu77=
ENST00000422678.2:c.168+62T= ENSP00000409326.2:n.168+62T=
ENST00000554470.5:c.57+173T= ENSP00000450862.1:n.57+173T=
ENST00000555765.5:c.179T= ENSP00000452451.1:p.Leu60=
ENST00000556161.1:c.179T= ENSP00000452188.1:p.Leu60=
NM_001243645.1:c.179T= NP_001230574.1:p.Leu60=
NM_021914.7:c.230T= NP_068733.1:p.Leu77=
NM_138638.4:c.230T= , LRG_213t1:c.230T= NP_619579.1:p.Leu77=
NR_028130.1:n.451+62T=
NR_028131.1:n.340+173T=
XM_011536363.1:c.179T= XP_011534665.1:p.Leu60=
XM_011536363.3:c.179T= XP_011534665.1:p.Leu60=
NM_138638.5:c.230T= MANE Select NP_619579.1:p.Leu77=
NM_001243645.2:c.179T= NP_001230574.1:p.Leu60=
NM_021914.8:c.230T= NP_068733.1:p.Leu77=
NR_028130.2:n.221+62T=
NR_028131.2:n.110+173T=