Canonical Allele Identifier: CA1138573318
Gene: FLNA HGNC NCBI

Linked Data

dbSNP Id: rs2067806950

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154371368_154371391dup , CM000685.2:g.154371368_154371391dup GRCh38
NC_000023.10:g.153599736_153599759dup , CM000685.1:g.153599736_153599759dup GRCh37
NC_000023.9:g.153252930_153252953dup NCBI36
NG_008677.1:g.1941_1964dup , LRG_745:g.1941_1964dup
NG_011506.1:g.8253_8276dup
NG_011506.2:g.8253_8276dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000369850.10:c.-116-25_-116-2dup MANE Select ENSP00000358866.3:n.-116-25_-116-2dup
ENST00000369850.7:c.-116-25_-116-2dup ENSP00000358866.3:n.-116-25_-116-2dup
ENST00000422373.5:c.-116-25_-116-2dup ENSP00000416926.1:n.-116-25_-116-2dup
ENST00000610817.4:c.-197-25_-197-2dup ENSP00000480593.1:n.-197-25_-197-2dup
NM_001110556.1:c.-116-25_-116-2dup NP_001104026.1:n.-116-25_-116-2dup
NM_001456.3:c.-116-25_-116-2dup NP_001447.2:n.-116-25_-116-2dup
XM_011531127.1:c.-116-25_-116-2dup XP_011529429.1:n.-116-25_-116-2dup
XM_011531128.1:c.-116-25_-116-2dup XP_011529430.1:n.-116-25_-116-2dup
XM_011531129.1:c.-116-25_-116-2dup XP_011529431.1:n.-116-25_-116-2dup
XM_011531130.1:c.-116-25_-116-2dup XP_011529432.1:n.-116-25_-116-2dup
XM_011531131.1:c.-116-25_-116-2dup XP_011529433.1:n.-116-25_-116-2dup
NM_001110556.2:c.-116-25_-116-2dup MANE Select NP_001104026.1:n.-116-25_-116-2dup
NM_001456.4:c.-116-25_-116-2dup NP_001447.2:n.-116-25_-116-2dup