Canonical Allele Identifier: CA241782

Gene: CFL2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.34713544C>T , CM000676.2:g.34713544C>T	GRCh38
NC_000014.8:g.35182750C>T , CM000676.1:g.35182750C>T	GRCh37
NC_000014.7:g.34252501C>T	NCBI36
NG_012740.1:g.6280G>A , LRG_213:g.6280G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298159.11:c.21G>A MANE Select	ENSP00000298159.6:p.Val7=
ENST00000341223.8:c.21G>A	ENSP00000340635.3:p.Val7=
ENST00000672163.1:c.21G>A	ENSP00000500375.1:p.Val7=
ENST00000672517.1:c.21G>A	ENSP00000500532.1:p.Val7=
ENST00000673315.1:c.-31G>A	ENSP00000500002.1:n.-31G>A
ENST00000298159.10:c.21G>A	ENSP00000298159.6:p.Val7=
ENST00000341223.7:c.21G>A	ENSP00000340635.3:p.Val7=
ENST00000422678.2:c.21G>A	ENSP00000409326.2:p.Val7=
ENST00000554470.5:c.21G>A	ENSP00000450862.1:p.Val7=
ENST00000555765.5:c.-31G>A	ENSP00000452451.1:n.-31G>A
ENST00000556161.1:c.-31G>A	ENSP00000452188.1:n.-31G>A
NM_001243645.1:c.-31G>A	NP_001230574.1:n.-31G>A
NM_021914.7:c.21G>A	NP_068733.1:p.Val7=
NM_138638.4:c.21G>A , LRG_213t1:c.21G>A	NP_619579.1:p.Val7=
NR_028130.1:n.304G>A
NR_028131.1:n.304G>A
XM_011536363.1:c.-31G>A	XP_011534665.1:n.-31G>A
XM_011536363.3:c.-31G>A	XP_011534665.1:n.-31G>A
NM_138638.5:c.21G>A MANE Select	NP_619579.1:p.Val7=
NM_001243645.2:c.-31G>A	NP_001230574.1:n.-31G>A
NM_021914.8:c.21G>A	NP_068733.1:p.Val7=
NR_028130.2:n.74G>A
NR_028131.2:n.74G>A