Canonical Allele Identifier: CA389421606

Gene: CFL2

Linked Data

• MyVariant Identifiers: chr14:g.35182509T>A (hg19) ; chr14:g.34713303T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.34713303T>A , CM000676.2:g.34713303T>A	GRCh38
NC_000014.8:g.35182509T>A , CM000676.1:g.35182509T>A	GRCh37
NC_000014.7:g.34252260T>A	NCBI36
NG_012740.1:g.6521A>T , LRG_213:g.6521A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298159.11:c.262A>T MANE Select	ENSP00000298159.6:p.Thr88Ser
ENST00000341223.8:c.262A>T	ENSP00000340635.3:p.Thr88Ser
ENST00000672163.1:c.262A>T	ENSP00000500375.1:p.Thr88Ser
ENST00000672517.1:c.262A>T	ENSP00000500532.1:p.Thr88Ser
ENST00000673315.1:c.211A>T	ENSP00000500002.1:p.Thr71Ser
ENST00000298159.10:c.262A>T	ENSP00000298159.6:p.Thr88Ser
ENST00000341223.7:c.262A>T	ENSP00000340635.3:p.Thr88Ser
ENST00000422678.2:c.168+94A>T	ENSP00000409326.2:n.168+94A>T
ENST00000554470.5:c.58-167A>T	ENSP00000450862.1:n.58-167A>T
ENST00000555765.5:c.211A>T	ENSP00000452451.1:p.Thr71Ser
ENST00000556161.1:c.211A>T	ENSP00000452188.1:p.Thr71Ser
NM_001243645.1:c.211A>T	NP_001230574.1:p.Thr71Ser
NM_021914.7:c.262A>T	NP_068733.1:p.Thr88Ser
NM_138638.4:c.262A>T , LRG_213t1:c.262A>T	NP_619579.1:p.Thr88Ser
NR_028130.1:n.451+94A>T
NR_028131.1:n.341-167A>T
XM_011536363.1:c.211A>T	XP_011534665.1:p.Thr71Ser
XM_011536363.3:c.211A>T	XP_011534665.1:p.Thr71Ser
NM_138638.5:c.262A>T MANE Select	NP_619579.1:p.Thr88Ser
NM_001243645.2:c.211A>T	NP_001230574.1:p.Thr71Ser
NM_021914.8:c.262A>T	NP_068733.1:p.Thr88Ser
NR_028130.2:n.221+94A>T
NR_028131.2:n.111-167A>T