Canonical Allele Identifier: CA389421823

Gene: CFL2

Linked Data

• gnomAD v4: 14-34713401-A-C
• MyVariant Identifiers: chr14:g.35182607A>C (hg19) ; chr14:g.34713401A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.34713401A>C , CM000676.2:g.34713401A>C	GRCh38
NC_000014.8:g.35182607A>C , CM000676.1:g.35182607A>C	GRCh37
NC_000014.7:g.34252358A>C	NCBI36
NG_012740.1:g.6423T>G , LRG_213:g.6423T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298159.11:c.164T>G MANE Select	ENSP00000298159.6:p.Ile55Ser
ENST00000341223.8:c.164T>G	ENSP00000340635.3:p.Ile55Ser
ENST00000672163.1:c.164T>G	ENSP00000500375.1:p.Ile55Ser
ENST00000672517.1:c.164T>G	ENSP00000500532.1:p.Ile55Ser
ENST00000673315.1:c.113T>G	ENSP00000500002.1:p.Ile38Ser
ENST00000298159.10:c.164T>G	ENSP00000298159.6:p.Ile55Ser
ENST00000341223.7:c.164T>G	ENSP00000340635.3:p.Ile55Ser
ENST00000422678.2:c.164T>G	ENSP00000409326.2:p.Ile55Ser
ENST00000554470.5:c.57+107T>G	ENSP00000450862.1:n.57+107T>G
ENST00000555765.5:c.113T>G	ENSP00000452451.1:p.Ile38Ser
ENST00000556161.1:c.113T>G	ENSP00000452188.1:p.Ile38Ser
NM_001243645.1:c.113T>G	NP_001230574.1:p.Ile38Ser
NM_021914.7:c.164T>G	NP_068733.1:p.Ile55Ser
NM_138638.4:c.164T>G , LRG_213t1:c.164T>G	NP_619579.1:p.Ile55Ser
NR_028130.1:n.447T>G
NR_028131.1:n.340+107T>G
XM_011536363.1:c.113T>G	XP_011534665.1:p.Ile38Ser
XM_011536363.3:c.113T>G	XP_011534665.1:p.Ile38Ser
NM_138638.5:c.164T>G MANE Select	NP_619579.1:p.Ile55Ser
NM_001243645.2:c.113T>G	NP_001230574.1:p.Ile38Ser
NM_021914.8:c.164T>G	NP_068733.1:p.Ile55Ser
NR_028130.2:n.217T>G
NR_028131.2:n.110+107T>G