Canonical Allele Identifier: CA2128728661

Gene: CFL2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.34713367G= , CM000676.2:g.34713367G=	GRCh38
NC_000014.8:g.35182573G= , CM000676.1:g.35182573G=	GRCh37
NC_000014.7:g.34252324G=	NCBI36
NG_012740.1:g.6457C= , LRG_213:g.6457C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298159.11:c.198C= MANE Select	ENSP00000298159.6:p.Asp66=
ENST00000341223.8:c.198C=	ENSP00000340635.3:p.Asp66=
ENST00000672163.1:c.198C=	ENSP00000500375.1:p.Asp66=
ENST00000672517.1:c.198C=	ENSP00000500532.1:p.Asp66=
ENST00000673315.1:c.147C=	ENSP00000500002.1:p.Asp49=
ENST00000298159.10:c.198C=	ENSP00000298159.6:p.Asp66=
ENST00000341223.7:c.198C=	ENSP00000340635.3:p.Asp66=
ENST00000422678.2:c.168+30C=	ENSP00000409326.2:n.168+30C=
ENST00000554470.5:c.57+141C=	ENSP00000450862.1:n.57+141C=
ENST00000555765.5:c.147C=	ENSP00000452451.1:p.Asp49=
ENST00000556161.1:c.147C=	ENSP00000452188.1:p.Asp49=
NM_001243645.1:c.147C=	NP_001230574.1:p.Asp49=
NM_021914.7:c.198C=	NP_068733.1:p.Asp66=
NM_138638.4:c.198C= , LRG_213t1:c.198C=	NP_619579.1:p.Asp66=
NR_028130.1:n.451+30C=
NR_028131.1:n.340+141C=
XM_011536363.1:c.147C=	XP_011534665.1:p.Asp49=
XM_011536363.3:c.147C=	XP_011534665.1:p.Asp49=
NM_138638.5:c.198C= MANE Select	NP_619579.1:p.Asp66=
NM_001243645.2:c.147C=	NP_001230574.1:p.Asp49=
NM_021914.8:c.198C=	NP_068733.1:p.Asp66=
NR_028130.2:n.221+30C=
NR_028131.2:n.110+141C=