Canonical Allele Identifier: CA7152356
Gene: CFL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.34713676T>G , CM000676.2:g.34713676T>G GRCh38
NC_000014.8:g.35182882T>G , CM000676.1:g.35182882T>G GRCh37
NC_000014.7:g.34252633T>G NCBI36
NG_012740.1:g.6148A>C , LRG_213:g.6148A>C

Transcript Alleles

HGVS Amino-acid Change
NM_138638.5:c.4-115A>C MANE Select NP_619579.1:n.4-115A>C
ENST00000298159.11:c.4-115A>C MANE Select ENSP00000298159.6:n.4-115A>C
NM_001243645.1:c.-48-115A>C NP_001230574.1:n.-48-115A>C
NM_001243645.2:c.-48-115A>C NP_001230574.1:n.-48-115A>C
NM_021914.7:c.1A>C NP_068733.1:p.Met1Leu
NM_021914.8:c.1A>C NP_068733.1:p.Met1Leu
NM_138638.4:c.4-115A>C , LRG_213t1:c.4-115A>C NP_619579.1:n.4-115A>C
NR_028130.1:n.287-115A>C
NR_028130.2:n.57-115A>C
NR_028131.1:n.287-115A>C
NR_028131.2:n.57-115A>C
ENST00000298159.10:c.4-115A>C ENSP00000298159.6:n.4-115A>C
ENST00000341223.7:c.1A>C ENSP00000340635.3:p.Met1Leu
ENST00000341223.8:c.1A>C ENSP00000340635.3:p.Met1Leu
ENST00000422678.2:c.4-115A>C ENSP00000409326.2:n.4-115A>C
ENST00000554470.5:c.4-115A>C ENSP00000450862.1:n.4-115A>C
ENST00000555765.5:c.-48-115A>C ENSP00000452451.1:n.-48-115A>C
ENST00000556161.1:c.-48-115A>C ENSP00000452188.1:n.-48-115A>C
ENST00000672163.1:c.1A>C ENSP00000500375.1:p.Met1Leu
ENST00000672517.1:c.1A>C ENSP00000500532.1:p.Met1Leu
ENST00000673315.1:c.-82A>C ENSP00000500002.1:n.-82A>C
XM_011536363.1:c.-48-115A>C XP_011534665.1:n.-48-115A>C
XM_011536363.3:c.-48-115A>C XP_011534665.1:n.-48-115A>C