Canonical Allele Identifier: CA389421592
Gene: CFL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.34713296T>G , CM000676.2:g.34713296T>G GRCh38
NC_000014.8:g.35182502T>G , CM000676.1:g.35182502T>G GRCh37
NC_000014.7:g.34252253T>G NCBI36
NG_012740.1:g.6528A>C , LRG_213:g.6528A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000298159.11:c.269A>C MANE Select ENSP00000298159.6:p.Glu90Ala
ENST00000341223.8:c.269A>C ENSP00000340635.3:p.Glu90Ala
ENST00000672163.1:c.269A>C ENSP00000500375.1:p.Glu90Ala
ENST00000672517.1:c.269A>C ENSP00000500532.1:p.Glu90Ala
ENST00000673315.1:c.218A>C ENSP00000500002.1:p.Glu73Ala
ENST00000298159.10:c.269A>C ENSP00000298159.6:p.Glu90Ala
ENST00000341223.7:c.269A>C ENSP00000340635.3:p.Glu90Ala
ENST00000422678.2:c.168+101A>C ENSP00000409326.2:n.168+101A>C
ENST00000554470.5:c.58-160A>C ENSP00000450862.1:n.58-160A>C
ENST00000555765.5:c.218A>C ENSP00000452451.1:p.Glu73Ala
ENST00000556161.1:c.218A>C ENSP00000452188.1:p.Glu73Ala
NM_001243645.1:c.218A>C NP_001230574.1:p.Glu73Ala
NM_021914.7:c.269A>C NP_068733.1:p.Glu90Ala
NM_138638.4:c.269A>C , LRG_213t1:c.269A>C NP_619579.1:p.Glu90Ala
NR_028130.1:n.451+101A>C
NR_028131.1:n.341-160A>C
XM_011536363.1:c.218A>C XP_011534665.1:p.Glu73Ala
XM_011536363.3:c.218A>C XP_011534665.1:p.Glu73Ala
NM_138638.5:c.269A>C MANE Select NP_619579.1:p.Glu90Ala
NM_001243645.2:c.218A>C NP_001230574.1:p.Glu73Ala
NM_021914.8:c.269A>C NP_068733.1:p.Glu90Ala
NR_028130.2:n.221+101A>C
NR_028131.2:n.111-160A>C