Canonical Allele Identifier: CA389421583
Gene: CFL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.34713293G>T , CM000676.2:g.34713293G>T GRCh38
NC_000014.8:g.35182499G>T , CM000676.1:g.35182499G>T GRCh37
NC_000014.7:g.34252250G>T NCBI36
NG_012740.1:g.6531C>A , LRG_213:g.6531C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000298159.11:c.272C>A MANE Select ENSP00000298159.6:p.Thr91Lys
ENST00000341223.8:c.272C>A ENSP00000340635.3:p.Thr91Lys
ENST00000672163.1:c.272C>A ENSP00000500375.1:p.Thr91Lys
ENST00000672517.1:c.272C>A ENSP00000500532.1:p.Thr91Lys
ENST00000673315.1:c.221C>A ENSP00000500002.1:p.Thr74Lys
ENST00000298159.10:c.272C>A ENSP00000298159.6:p.Thr91Lys
ENST00000341223.7:c.272C>A ENSP00000340635.3:p.Thr91Lys
ENST00000422678.2:c.168+104C>A ENSP00000409326.2:n.168+104C>A
ENST00000554470.5:c.58-157C>A ENSP00000450862.1:n.58-157C>A
ENST00000555765.5:c.221C>A ENSP00000452451.1:p.Thr74Lys
ENST00000556161.1:c.221C>A ENSP00000452188.1:p.Thr74Lys
NM_001243645.1:c.221C>A NP_001230574.1:p.Thr74Lys
NM_021914.7:c.272C>A NP_068733.1:p.Thr91Lys
NM_138638.4:c.272C>A , LRG_213t1:c.272C>A NP_619579.1:p.Thr91Lys
NR_028130.1:n.451+104C>A
NR_028131.1:n.341-157C>A
XM_011536363.1:c.221C>A XP_011534665.1:p.Thr74Lys
XM_011536363.3:c.221C>A XP_011534665.1:p.Thr74Lys
NM_138638.5:c.272C>A MANE Select NP_619579.1:p.Thr91Lys
NM_001243645.2:c.221C>A NP_001230574.1:p.Thr74Lys
NM_021914.8:c.272C>A NP_068733.1:p.Thr91Lys
NR_028130.2:n.221+104C>A
NR_028131.2:n.111-157C>A