Canonical Allele Identifier: CA353333432
Gene: FLNB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.58077196G>C , CM000665.2:g.58077196G>C GRCh38
NC_000003.11:g.58062923G>C , CM000665.1:g.58062923G>C GRCh37
NC_000003.10:g.58037963G>C NCBI36
NG_012801.1:g.73797G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682097.1:c.443G>C ENSP00000508183.1:p.Trp148Ser
ENST00000682868.1:n.586G>C
ENST00000682871.1:c.443G>C ENSP00000507805.1:p.Trp148Ser
ENST00000682987.1:n.586G>C
ENST00000683511.1:n.602G>C
ENST00000684107.1:c.443G>C ENSP00000507440.1:p.Trp148Ser
ENST00000684506.1:c.443G>C ENSP00000507728.1:p.Trp148Ser
ENST00000684517.1:c.443G>C ENSP00000507828.1:p.Trp148Ser
ENST00000684607.1:c.443G>C ENSP00000508224.1:p.Trp148Ser
ENST00000295956.9:c.443G>C MANE Select ENSP00000295956.5:p.Trp148Ser
ENST00000295956.8:c.443G>C ENSP00000295956.4:p.Trp148Ser
ENST00000358537.7:c.443G>C ENSP00000351339.3:p.Trp148Ser
ENST00000429972.6:c.443G>C ENSP00000415599.2:p.Trp148Ser
ENST00000490882.5:c.443G>C ENSP00000420213.1:p.Trp148Ser
NM_001164317.1:c.443G>C NP_001157789.1:p.Trp148Ser
NM_001164318.1:c.443G>C NP_001157790.1:p.Trp148Ser
NM_001164319.1:c.443G>C NP_001157791.1:p.Trp148Ser
NM_001457.3:c.443G>C NP_001448.2:p.Trp148Ser
XM_005264977.1:c.443G>C XP_005265034.1:p.Trp148Ser
XM_005264978.1:c.443G>C XP_005265035.1:p.Trp148Ser
XM_005264981.1:c.443G>C XP_005265038.1:p.Trp148Ser
XR_940396.1:n.588G>C
XM_005264978.2:c.443G>C XP_005265035.1:p.Trp148Ser
XR_001740065.1:n.588G>C
XR_940396.2:n.588G>C
NM_001164317.2:c.443G>C NP_001157789.1:p.Trp148Ser
NM_001164318.2:c.443G>C NP_001157790.1:p.Trp148Ser
NM_001164319.2:c.443G>C NP_001157791.1:p.Trp148Ser
NM_001457.4:c.443G>C MANE Select NP_001448.2:p.Trp148Ser