Canonical Allele Identifier: CA389421259

Gene: CFL2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.34713093T>A , CM000676.2:g.34713093T>A	GRCh38
NC_000014.8:g.35182299T>A , CM000676.1:g.35182299T>A	GRCh37
NC_000014.7:g.34252050T>A	NCBI36
NG_012740.1:g.6731A>T , LRG_213:g.6731A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298159.11:c.355A>T MANE Select	ENSP00000298159.6:p.Ser119Cys
ENST00000341223.8:c.355A>T	ENSP00000340635.3:p.Ser119Cys
ENST00000672163.1:c.355A>T	ENSP00000500375.1:p.Ser119Cys
ENST00000672517.1:c.355A>T	ENSP00000500532.1:p.Ser119Cys
ENST00000673315.1:c.304A>T	ENSP00000500002.1:p.Ser102Cys
ENST00000298159.10:c.355A>T	ENSP00000298159.6:p.Ser119Cys
ENST00000341223.7:c.355A>T	ENSP00000340635.3:p.Ser119Cys
ENST00000422678.2:c.*35A>T	ENSP00000409326.2:n.*35A>T
ENST00000554470.5:c.*35A>T	ENSP00000450862.1:n.*35A>T
ENST00000555765.5:c.304A>T	ENSP00000452451.1:p.Ser102Cys
ENST00000556161.1:c.304A>T	ENSP00000452188.1:p.Ser102Cys
NM_001243645.1:c.304A>T	NP_001230574.1:p.Ser102Cys
NM_021914.7:c.355A>T	NP_068733.1:p.Ser119Cys
NM_138638.4:c.355A>T , LRG_213t1:c.355A>T	NP_619579.1:p.Ser119Cys
NR_028130.1:n.495A>T
NR_028131.1:n.384A>T
XM_011536363.1:c.304A>T	XP_011534665.1:p.Ser102Cys
XM_011536363.3:c.304A>T	XP_011534665.1:p.Ser102Cys
NM_138638.5:c.355A>T MANE Select	NP_619579.1:p.Ser119Cys
NM_001243645.2:c.304A>T	NP_001230574.1:p.Ser102Cys
NM_021914.8:c.355A>T	NP_068733.1:p.Ser119Cys
NR_028130.2:n.265A>T
NR_028131.2:n.154A>T