Canonical Allele Identifier: CA389421105

Gene: CFL2

Linked Data

• ClinVar Variation Id: 465805
• ClinVar RCV Id: RCV000538686
• dbSNP Id: rs1555333750
• MyVariant Identifiers: chr14:g.35182192del (hg19) ; chr14:g.34712986del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.34712991del , CM000676.2:g.34712991del	GRCh38
NC_000014.8:g.35182197del , CM000676.1:g.35182197del	GRCh37
NC_000014.7:g.34251948del	NCBI36
NG_012740.1:g.6838del , LRG_213:g.6838del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298159.11:c.389-9del MANE Select	ENSP00000298159.6:n.389-9del
ENST00000341223.8:c.389-9del	ENSP00000340635.3:n.389-9del
ENST00000672163.1:c.389-9del	ENSP00000500375.1:n.389-9del
ENST00000672517.1:c.389-9del	ENSP00000500532.1:n.389-9del
ENST00000673315.1:c.338-9del	ENSP00000500002.1:n.338-9del
ENST00000298159.10:c.389-9del	ENSP00000298159.6:n.389-9del
ENST00000341223.7:c.389-9del	ENSP00000340635.3:n.389-9del
ENST00000422678.2:c.*69-9del	ENSP00000409326.2:n.*69-9del
ENST00000554470.5:c.*69-9del	ENSP00000450862.1:n.*69-9del
ENST00000555765.5:c.338-9del	ENSP00000452451.1:n.338-9del
ENST00000556161.1:c.338-9del	ENSP00000452188.1:n.338-9del
NM_001243645.1:c.338-9del	NP_001230574.1:n.338-9del
NM_021914.7:c.389-9del	NP_068733.1:n.389-9del
NM_138638.4:c.389-9del , LRG_213t1:c.389-9del	NP_619579.1:n.389-9del
NR_028130.1:n.529-9del
NR_028131.1:n.418-9del
XM_011536363.1:c.338-9del	XP_011534665.1:n.338-9del
XM_011536363.3:c.338-9del	XP_011534665.1:n.338-9del
NM_138638.5:c.389-9del MANE Select	NP_619579.1:n.389-9del
NM_001243645.2:c.338-9del	NP_001230574.1:n.338-9del
NM_021914.8:c.389-9del	NP_068733.1:n.389-9del
NR_028130.2:n.299-9del
NR_028131.2:n.188-9del