Canonical Allele Identifier: CA389422084
Gene: CFL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.34713511C>T , CM000676.2:g.34713511C>T GRCh38
NC_000014.8:g.35182717C>T , CM000676.1:g.35182717C>T GRCh37
NC_000014.7:g.34252468C>T NCBI36
NG_012740.1:g.6313G>A , LRG_213:g.6313G>A

Transcript Alleles

HGVS Amino-acid Change
NM_138638.5:c.54G>A MANE Select NP_619579.1:p.Met18Ile
ENST00000298159.11:c.54G>A MANE Select ENSP00000298159.6:p.Met18Ile
NM_001243645.1:c.3G>A NP_001230574.1:p.Met1Ile
NM_001243645.2:c.3G>A NP_001230574.1:p.Met1Ile
NM_021914.7:c.54G>A NP_068733.1:p.Met18Ile
NM_021914.8:c.54G>A NP_068733.1:p.Met18Ile
NM_138638.4:c.54G>A , LRG_213t1:c.54G>A NP_619579.1:p.Met18Ile
NR_028130.1:n.337G>A
NR_028130.2:n.107G>A
NR_028131.1:n.337G>A
NR_028131.2:n.107G>A
ENST00000298159.10:c.54G>A ENSP00000298159.6:p.Met18Ile
ENST00000341223.7:c.54G>A ENSP00000340635.3:p.Met18Ile
ENST00000341223.8:c.54G>A ENSP00000340635.3:p.Met18Ile
ENST00000422678.2:c.54G>A ENSP00000409326.2:p.Met18Ile
ENST00000554470.5:c.54G>A ENSP00000450862.1:p.Met18Ile
ENST00000555765.5:c.3G>A ENSP00000452451.1:p.Met1Ile
ENST00000556161.1:c.3G>A ENSP00000452188.1:p.Met1Ile
ENST00000672163.1:c.54G>A ENSP00000500375.1:p.Met18Ile
ENST00000672517.1:c.54G>A ENSP00000500532.1:p.Met18Ile
ENST00000673315.1:c.3G>A ENSP00000500002.1:p.Met1Ile
XM_011536363.1:c.3G>A XP_011534665.1:p.Met1Ile
XM_011536363.3:c.3G>A XP_011534665.1:p.Met1Ile