Canonical Allele Identifier: CA2824295708
Gene: FLNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154371326_154371327insC , CM000685.2:g.154371326_154371327insC GRCh38
NC_000023.10:g.153599694_153599695insC , CM000685.1:g.153599694_153599695insC GRCh37
NC_000023.9:g.153252888_153252889insC NCBI36
NG_008677.1:g.1899_1900insC , LRG_745:g.1899_1900insC
NG_011506.1:g.8312_8313insG
NG_011506.2:g.8312_8313insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000369850.10:c.-82_-81insG MANE Select ENSP00000358866.3:n.-82_-81insG
ENST00000369850.7:c.-82_-81insG ENSP00000358866.3:n.-82_-81insG
ENST00000422373.5:c.-82_-81insG ENSP00000416926.1:n.-82_-81insG
ENST00000610817.4:c.-163_-162insG ENSP00000480593.1:n.-163_-162insG
NM_001110556.1:c.-82_-81insG NP_001104026.1:n.-82_-81insG
NM_001456.3:c.-82_-81insG NP_001447.2:n.-82_-81insG
XM_011531127.1:c.-82_-81insG XP_011529429.1:n.-82_-81insG
XM_011531128.1:c.-82_-81insG XP_011529430.1:n.-82_-81insG
XM_011531129.1:c.-82_-81insG XP_011529431.1:n.-82_-81insG
XM_011531130.1:c.-82_-81insG XP_011529432.1:n.-82_-81insG
XM_011531131.1:c.-82_-81insG XP_011529433.1:n.-82_-81insG
NM_001110556.2:c.-82_-81insG MANE Select NP_001104026.1:n.-82_-81insG
NM_001456.4:c.-82_-81insG NP_001447.2:n.-82_-81insG