Canonical Allele Identifier: CA389421830
Gene: CFL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.34713404T>A , CM000676.2:g.34713404T>A GRCh38
NC_000014.8:g.35182610T>A , CM000676.1:g.35182610T>A GRCh37
NC_000014.7:g.34252361T>A NCBI36
NG_012740.1:g.6420A>T , LRG_213:g.6420A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000298159.11:c.161A>T MANE Select ENSP00000298159.6:p.Gln54Leu
ENST00000341223.8:c.161A>T ENSP00000340635.3:p.Gln54Leu
ENST00000672163.1:c.161A>T ENSP00000500375.1:p.Gln54Leu
ENST00000672517.1:c.161A>T ENSP00000500532.1:p.Gln54Leu
ENST00000673315.1:c.110A>T ENSP00000500002.1:p.Gln37Leu
ENST00000298159.10:c.161A>T ENSP00000298159.6:p.Gln54Leu
ENST00000341223.7:c.161A>T ENSP00000340635.3:p.Gln54Leu
ENST00000422678.2:c.161A>T ENSP00000409326.2:p.Gln54Leu
ENST00000554470.5:c.57+104A>T ENSP00000450862.1:n.57+104A>T
ENST00000555765.5:c.110A>T ENSP00000452451.1:p.Gln37Leu
ENST00000556161.1:c.110A>T ENSP00000452188.1:p.Gln37Leu
NM_001243645.1:c.110A>T NP_001230574.1:p.Gln37Leu
NM_021914.7:c.161A>T NP_068733.1:p.Gln54Leu
NM_138638.4:c.161A>T , LRG_213t1:c.161A>T NP_619579.1:p.Gln54Leu
NR_028130.1:n.444A>T
NR_028131.1:n.340+104A>T
XM_011536363.1:c.110A>T XP_011534665.1:p.Gln37Leu
XM_011536363.3:c.110A>T XP_011534665.1:p.Gln37Leu
NM_138638.5:c.161A>T MANE Select NP_619579.1:p.Gln54Leu
NM_001243645.2:c.110A>T NP_001230574.1:p.Gln37Leu
NM_021914.8:c.161A>T NP_068733.1:p.Gln54Leu
NR_028130.2:n.214A>T
NR_028131.2:n.110+104A>T